Large

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.  

Science & Healthcare

AbbVie

You must have a health-related qualification, 1+ year clinical experience (Oncology preferred), knowledge of ICH/GCP, strong organizational skills, fluency in English and Italian, and travel availability.

You will monitor clinical sites, ensure protocol compliance, conduct site visits, train personnel, manage payments, and recommend potential investigators while ensuring data quality and safety.

Research & Development

Healthcare

Rome

<div>
 Company Description
 AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
 To enable AbbVie’ s emergence as a world class R&amp;D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies.
 Key Responsibilities:
 <ul>
 <li>Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.</li>
 <li>Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.</li>
 <li>Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.</li>
 <li>Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.</li>
 <li>Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.</li>
 <li>Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.</li>
 <li>Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.</li>
 <li>Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.</li>
 </ul> Qualifications
 Requirements:
 <ul>
 <li>Appropriate tertiary qualification, health related (e.g., Medical, Scientific) preferred.</li>
 <li>Minimum of 1 year of clinically-related experience. A previous experience in Oncology is a plus.</li>
 <li>Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.</li>
 <li>Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.</li>
 <li>Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.</li>
 <li>Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.</li>
 <li>Demonstrated business ethics and integrity.</li>
 <li>Fluency both in English and Italian</li>
 <li>Availabiity to travel</li>
 </ul> Additional Information
 Il presente annuncio è rivolto ad entrambi i sessi, ai sensi delle leggi 903/77 e 125/91, e a persone di tutte le età e tutte le nazionalità, ai sensi dei decreti legislativi 215/03 e 216/03.I dati personali contenuti nei c.v. saranno trattati e conservati esclusivamente per finalità di selezione, nel rispetto del D.lgs.vo 196/2003 e s.m.i e del Regolamento (UE) 2016/679.
 <div></div>
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html
</div>


 Company Description
  AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
  To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies.
  Key Responsibilities:
 
  Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
  Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
  Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
  Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
  Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
  Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
  Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
  Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.
   Qualifications
  Requirements:
 
  Appropriate tertiary qualification, health related (e.g., Medical, Scientific) preferred.
  Minimum of 1 year of clinically-related experience. A previous experience in Oncology is a plus.
  Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
  Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
  Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
  Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
  Demonstrated business ethics and integrity.
  Fluency both in English and Italian
  Availabiity to travel
   Additional Information
  Il presente annuncio è rivolto ad entrambi i sessi, ai sensi delle leggi 903/77 e 125/91, e a persone di tutte le età e tutte le nazionalità, ai sensi dei decreti legislativi 215/03 e 216/03.I dati personali contenuti nei c.v. saranno trattati e conservati esclusivamente per finalità di selezione, nel rispetto del D.lgs.vo 196/2003 e s.m.i e del Regolamento (UE) 2016/679.
 
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html


Clinical Research Associate II - AbbVie

Clinical Research Associate II

You must be pursuing a relevant bachelor's degree with a graduation date between Dec 2025 - June 2026, have leadership skills, excellent communication, and be willing to travel.

You will engage in product optimization, conduct quality data analysis, optimize enzyme synthesis, and rotate through various operations assignments in manufacturing and safety.

Engineering

Irvine

<div>
 Company Description
 AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
 Envision spending your summer working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for participants in the Operations Development Program Internship at AbbVie.
 Operations Development Program Internship Description:
 As an AbbVie Operations intern, you will participate in a paid, ten-to-twelve-week summer program working on meaningful assignments that have a real impact on our business and patients worldwide. AbbVie’s global Operations business offers you an opportunity to work in a variety of fields based on your degree type.
 Past examples of projects have included:
 <ul>
 <li>Product and process optimization in a manufacturing facility</li>
 <li>Quality systems data analysis to identify compliance trends</li>
 <li>Optimize an enzyme to catalyze a challenging step in the synthesis of a recently approved product</li>
 </ul>
 AbbVie’s worldwide business offers you an opportunity for a variety of potential work experiences that are aligned to a variety of functional areas, including those listed below. Interns will be placed in assignments based on business needs and skill set.
 <ul>
 <li>Manufacturing</li>
 <li>Engineering</li>
 <li>Quality</li>
 <li>Science &amp; Technology</li>
 <li>Environmental Health and Safety</li>
 </ul>
 Locations:
 Interns will be placed in one of the following U.S locations. Interns will be placed based on business need and background.
 <ul>
 <li>Branchburg, New Jersey</li>
 <li>Irvine, California</li>
 <li>Lake County, IL</li>
 <li>Waco, Texas</li>
 <li>Worcester, Massachusetts</li>
 </ul>
 AbbVie strongly considers high performing interns as candidates for their Operations Development Program (ODP) after they graduate. AbbVie’s ODP is a three-year rotational program with three separate work assignments. The rotations are carried out in a variety of functional areas within Operations. The goal of the program is to develop AbbVie’s future leaders, provide exposure across the business on a global scale, and forums for skill and professional development. If you are interested and want more information visit www.abbviecareers.com and look under student opportunities. Qualifications
 Minimum Qualifications:
 <ul>
 <li>Must be currently enrolled in university, pursuing a bachelor's degree in Chemistry, Analytical Chemistry, Chemical Engineering, Mechanical Engineering, or related major.</li>
 <li>Expected graduation date between Dec 2025 - June 2026.</li>
 <li>Demonstrated leadership skills (i.e., extracurricular activities or projects).</li>
 <li>Mobility is a key requirement as a pipeline internship to our Operations Development Program. Operations Development Program Members will be required to experience at least one assignment based in one of our U.S. Operations Plants and will rotate to different sites with each rotation based on business need.</li>
 </ul>
 Preferred Qualifications:
 <ul>
 <li>Excellent problem-solving, written, and verbal skills.</li>
 <li>Exceptional interpersonal, leadership and project management skills.</li>
 <li>Proven track record of teamwork, adaptability, innovation, initiative, and integrity.</li>
 </ul>
 Equal Employment Opportunity
 At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. Additional Information
 Benefits and Amenities
 <ul>
 <li>Competitive pay</li>
 <li>Relocation support for eligible students</li>
 <li>Select wellness benefits and paid holiday / sick time</li>
 </ul>
 Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
 <ul>
 <li>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.</li>
 </ul>
 Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
 <div></div>
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html
</div>


 Company Description
  AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
  Envision spending your summer working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for participants in the Operations Development Program Internship at AbbVie.
  Operations Development Program Internship Description:
 As an AbbVie Operations intern, you will participate in a paid, ten-to-twelve-week summer program working on meaningful assignments that have a real impact on our business and patients worldwide. AbbVie’s global Operations business offers you an opportunity to work in a variety of fields based on your degree type.
  Past examples of projects have included:
 
  Product and process optimization in a manufacturing facility
  Quality systems data analysis to identify compliance trends
  Optimize an enzyme to catalyze a challenging step in the synthesis of a recently approved product
 
 AbbVie’s worldwide business offers you an opportunity for a variety of potential work experiences that are aligned to a variety of functional areas, including those listed below. Interns will be placed in assignments based on business needs and skill set.
 
  Manufacturing
  Engineering
  Quality
  Science & Technology
  Environmental Health and Safety
 
  Locations:
 Interns will be placed in one of the following U.S locations. Interns will be placed based on business need and background.
 
  Branchburg, New Jersey
  Irvine, California
  Lake County, IL
  Waco, Texas
  Worcester, Massachusetts
 
 AbbVie strongly considers high performing interns as candidates for their Operations Development Program (ODP) after they graduate. AbbVie’s ODP is a three-year rotational program with three separate work assignments. The rotations are carried out in a variety of functional areas within Operations. The goal of the program is to develop AbbVie’s future leaders, provide exposure across the business on a global scale, and forums for skill and professional development. If you are interested and want more information visit www.abbviecareers.com and look under student opportunities. Qualifications
  Minimum Qualifications:
 
  Must be currently enrolled in university, pursuing a bachelor's degree in Chemistry, Analytical Chemistry, Chemical Engineering, Mechanical Engineering, or related major.
  Expected graduation date between Dec 2025 - June 2026.
  Demonstrated leadership skills (i.e., extracurricular activities or projects).
  Mobility is a key requirement as a pipeline internship to our Operations Development Program. Operations Development Program Members will be required to experience at least one assignment based in one of our U.S. Operations Plants and will rotate to different sites with each rotation based on business need.
 
  Preferred Qualifications:
 
  Excellent problem-solving, written, and verbal skills.
  Exceptional interpersonal, leadership and project management skills.
  Proven track record of teamwork, adaptability, innovation, initiative, and integrity.
 
  Equal Employment Opportunity
 At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. Additional Information
  Benefits and Amenities
 
  Competitive pay
  Relocation support for eligible students
  Select wellness benefits and paid holiday / sick time
 
 Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
 
  The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
 
 Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
 
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html


2025 Operations Intern - AbbVie

2025 Operations Intern

You need a Bachelor's degree, 3-5 years in pharma/biotech marketing, oncology experience, Gulf market knowledge, fluent in English (Arabic preferred), and strong strategic and financial skills.

You will collaborate with teams to define brand strategy, ensure patient-centricity, guide marketing activities, manage budgets, develop performance metrics, and foster team collaboration.

Sales & Business Development

Marketing

Dubai

<div>
 Company Description
 AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
 Purpose Statement:
 <ul>
 <li>The oncology brand Manager – Gulf main responsibility is to Lead the comprehension of patient experience insights across the Brand and In Field Team and develop the Patient Journey to focus the Brand Team on the delivery of patient-centric strategies including CLM engagement and customization within AbbVie business code of conduct, policies and all applicable laws and regulations.</li>
 </ul>
 
 Major Responsibilities:
 <ul>
 <li>Collaborate with Brand Team and In-Field Team members, facilitate cross-stakeholder discussions (with Health Care Professional (HCP) and non-HCP stakeholders) and synthesize the insights gained to identify target segments, to determine brand positioning, to drive Close Loop Marketing engagement and customization and to populate Brand Plan Insights Chapter.</li>
 <li>Secure input and cross stakeholder viewpoints to develop a robust and accurate Patient Journey; propose strategic objectives for the Brand Team review based on Patient Journey findings and challenge and critique Brand Team strategies in order to ensure patient-centricity.</li>
 <li>Ensure all functional deliverables are consistent with branding and deliver emotional messages aligned to Brand Story.</li>
 <li>Guide the design and implementation of all marketing activities and include innovative marketing tactics, traditional and non-traditional partnerships, multi-channel opportunities and multi-stakeholder initiatives to meet strategic brand objectives.</li>
 <li>Ensure all in-field materials, strategies and tactics are aligned in order to drive momentum of strategic brand objectives.</li>
 <li>Lead the development of marketing inputs to Strategic Brand Plan, consolidate the 1-year Tactical Brand Plan and coordinate preparation of the Long-Range Plan to drive brand success.</li>
 <li>Develop, lead and coach direct reports (if applicable), forecast, monitor brand KPIs, manage budget and brand P&amp;L (if applicable), track ROI measurements for all marketing activities to achieve or exceed brand plan objectives. </li>
 </ul>
 As Brand Team Lead (if applicable)
 <ul>
 <li>Lead the Brand Team around a brand vision and objectives that are shared by all members.</li>
 <li>Ensure Brand Team Members contribute to the development of the Brand strategy through the Brand Planning process in line with strategy defined by Global Brand Team and ensure adequate involvement of multiple functions as relevant for the Brand objectives.</li>
 <li>Continuously encourage Brand Team members’ collaboration and foster team spirit.</li>
 <li>Take accountability and responsibility for Brand Team activities and processes (organize / chair / facilitate Brand Team meetings</li>
 </ul>
 
 Here is to know more about AbbVie Oncology Pipeline. https://www.abbvie.com/science/pipeline.html Qualifications
 Qualifications:
 Basic:
 <ul>
 <li>Bachelor’s degree or equivalent</li>
 <li>Oncology- Solid Tumors experience is a must</li>
 <li>Knowledge of Gulf market is preferred</li>
 <li>Minimum of 3-5 years marketing experience in Pharmaceutical and/or Medical Device Industry</li>
 <li>Relevant experience with proven track record of success in marketing within biotech/pharmaceutical industry</li>
 <li>Fluency in English and preferably Arabic</li>
 <li>Ability to translate strategies into actionable and realistic marketing actions</li>
 <li>Ability to lead, motivate and coordinate cross functional teams</li>
 <li>Solid working knowledge of healthcare environment and evolving landscape</li>
 <li>Solid knowledge of strategic and tactical marketing principles and techniques including digital knowledge</li>
 <li>Solid knowledge on finance principles and processes</li>
 <li>English language proficiency verbally and in writing (for all non-English speaking countries)</li>
 </ul>
 Additional Information
 Key Stakeholders:
 External: Patients, Health Care Professionals, Key Opinion Leaders, payers, agencies (MR, PR, digital)
 Internal: In-field teams, Brand Team, Brand Team Leader, Area Commercial, Affiliate Management Team
 <div></div>
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html
</div>


 Company Description
  AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
  Purpose Statement:
 
  The oncology brand Manager – Gulf main responsibility is to Lead the comprehension of patient experience insights across the Brand and In Field Team and develop the Patient Journey to focus the Brand Team on the delivery of patient-centric strategies including CLM engagement and customization within AbbVie business code of conduct, policies and all applicable laws and regulations.
 
 
  Major Responsibilities:
 
  Collaborate with Brand Team and In-Field Team members, facilitate cross-stakeholder discussions (with Health Care Professional (HCP) and non-HCP stakeholders) and synthesize the insights gained to identify target segments, to determine brand positioning, to drive Close Loop Marketing engagement and customization and to populate Brand Plan Insights Chapter.
  Secure input and cross stakeholder viewpoints to develop a robust and accurate Patient Journey; propose strategic objectives for the Brand Team review based on Patient Journey findings and challenge and critique Brand Team strategies in order to ensure patient-centricity.
  Ensure all functional deliverables are consistent with branding and deliver emotional messages aligned to Brand Story.
  Guide the design and implementation of all marketing activities and include innovative marketing tactics, traditional and non-traditional partnerships, multi-channel opportunities and multi-stakeholder initiatives to meet strategic brand objectives.
  Ensure all in-field materials, strategies and tactics are aligned in order to drive momentum of strategic brand objectives.
  Lead the development of marketing inputs to Strategic Brand Plan, consolidate the 1-year Tactical Brand Plan and coordinate preparation of the Long-Range Plan to drive brand success.
  Develop, lead and coach direct reports (if applicable), forecast, monitor brand KPIs, manage budget and brand P&L (if applicable), track ROI measurements for all marketing activities to achieve or exceed brand plan objectives. 
 
 As Brand Team Lead (if applicable)
 
  Lead the Brand Team around a brand vision and objectives that are shared by all members.
  Ensure Brand Team Members contribute to the development of the Brand strategy through the Brand Planning process in line with strategy defined by Global Brand Team and ensure adequate involvement of multiple functions as relevant for the Brand objectives.
  Continuously encourage Brand Team members’ collaboration and foster team spirit.
  Take accountability and responsibility for Brand Team activities and processes (organize / chair / facilitate Brand Team meetings
 
 
  Here is to know more about AbbVie Oncology Pipeline. https://www.abbvie.com/science/pipeline.html Qualifications
  Qualifications:
 Basic:
 
  Bachelor’s degree or equivalent
  Oncology- Solid Tumors experience is a must
  Knowledge of Gulf market is preferred
  Minimum of 3-5 years marketing experience in Pharmaceutical and/or Medical Device Industry
  Relevant experience with proven track record of success in marketing within biotech/pharmaceutical industry
  Fluency in English and preferably Arabic
  Ability to translate strategies into actionable and realistic marketing actions
  Ability to lead, motivate and coordinate cross functional teams
  Solid working knowledge of healthcare environment and evolving landscape
  Solid knowledge of strategic and tactical marketing principles and techniques including digital knowledge
  Solid knowledge on finance principles and processes
  English language proficiency verbally and in writing (for all non-English speaking countries)
 
  Additional Information
  Key Stakeholders:
 External: Patients, Health Care Professionals, Key Opinion Leaders, payers, agencies (MR, PR, digital)
 Internal: In-field teams, Brand Team, Brand Team Leader, Area Commercial, Affiliate Management Team
 
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html


Oncology Brand Manager - Gulf - AbbVie

Oncology Brand Manager - Gulf

You need a doctorate or MSc, MSL experience preferred, knowledge of biotech/pharma, strong communication skills, tech-savvy, and ability to engage stakeholders effectively.

You will engage with healthcare professionals, support studies, deliver scientific presentations, identify collaborators, and summarize key data from scientific meetings.

Science

Calgary

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Joining AbbVie means, you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada whereby 90% of our employees are proud to say they work for AbbVie and 88% are proud of how we contribute to the community. AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. When choosing your career path, choose to be remarkable. We have a new opportunity for a Medical Science Liaison (MSL) to join our Medical Affairs team. In this exciting career opportunity, you will develop and nurture relationships, as well as advance our scientific credibility with established and emerging external experts (EEs). Our MSLs respond to requests by providing key scientific/medical information to external experts and internal stakeholders. This role will cover BC and Alberta. Key Responsibilities: * Develop/maintain key scientific knowledge that enables credible dissemination of information to external experts (EEs) and other healthcare professionals (HCPs), to help the development of professional working relationships. * Participate and follow-up on assigned investigator-initiated studies (IIS), clinical studies and medical projects initiated within the relevant therapeutic area (TA). * Provide scientific support and help maintain relationships with external experts/academic centers. * Deliver credible presentations on scientific matters to HCPs, individually or in groups. * Participate in the selection process to identify qualified HCPs AbbVie would wish to engage in collaborative efforts – such as research, or lecture/meeting support (advisory boards, congresses, symposiums, etc.); and to ensure a high level of scientific or educational integrity in these collaborative efforts. * Attend relevant scientific meetings/conferences and develop summaries of key data presented. Qualifications Education/Experience Required: * Doctorate or MD or MSc degree in scientific related discipline and demonstrated experience. * Relevant business experience with solid knowledge of the biotech/pharmaceutical industry. * Previous experience as an MSL preferred.Relevant. Previous experience in a customer-facing role in the healthcare industry.Experience in the presentation and/or interpretation of scientific or clinical research publications. * Knowledge of scientific methods applied to clinical research and the current legislative/regulatory controls. * Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and medical research in general. Essential Skills & Abilities: * English language proficiency (oral and written). * Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.) * Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks). * Travel required about 30% of the time. * Valid driver’s license and passport. Key in-Field Team (IFT) Competencies: * Ability to understand the unmet needs of key stakeholders, make decisions that have an impact and execute the integration and assimilation of that information into the IFTs’ engagement approach. * Ability to coordinate scientific/medical engagement efforts across stakeholders within a single account, to develop interaction plans that are inline with the Scientific Interaction Plan (SIP) to achieve medical objectives. * In-depth understanding and execution of meaningful strategies and data-based business decisions to exceed IFT business goals. * Effectively communicate, collaborate, and incorporate the views of other in-field team members to optimize business objectives. AbbVie is an equal opportunity employer and encourages women, Aboriginal people, persons with disabilities and members of visible minorities to apply. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.Job DescriptionJoining AbbVie means, you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada whereby 90% of our employees are proud to say they work for AbbVie and 88% are proud of how we contribute to the community.AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio.When choosing your career path, choose to be remarkable.We have a new opportunity for a Medical Science Liaison (MSL) to join our Medical Affairs team. In this exciting career opportunity, you will develop and nurture relationships, as well as advance our scientific credibility with established and emerging external experts (EEs). Our MSLs respond to requests by providing key scientific/medical information to external experts and internal stakeholders. This role will cover BC and Alberta.Key Responsibilities: * Develop/maintain key scientific knowledge that enables credible dissemination of information to external experts (EEs) and other healthcare professionals (HCPs), to help the development of professional working relationships. * Participate and follow-up on assigned investigator-initiated studies (IIS), clinical studies and medical projects initiated within the relevant therapeutic area (TA). * Provide scientific support and help maintain relationships with external experts/academic centers. * Deliver credible presentations on scientific matters to HCPs, individually or in groups. * Participate in the selection process to identify qualified HCPs AbbVie would wish to engage in collaborative efforts – such as research, or lecture/meeting support (advisory boards, congresses, symposiums, etc.); and to ensure a high level of scientific or educational integrity in these collaborative efforts. * Attend relevant scientific meetings/conferences and develop summaries of key data presented.      QualificationsEducation/Experience Required: * Doctorate or MD or MSc degree in scientific related discipline and demonstrated experience. * Relevant business experience with solid knowledge of the biotech/pharmaceutical industry.    * Previous experience as an MSL preferred.Relevant. Previous experience in a customer-facing role in the healthcare industry.Experience in the presentation and/or interpretation of scientific or clinical research publications. * Knowledge of scientific methods applied to clinical research and the current legislative/regulatory controls. * Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and medical research in general.      Essential Skills & Abilities: * English language proficiency (oral and written). * Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.) * Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks). * Travel required about 30% of the time. * Valid driver’s license and passport.      Key in-Field Team (IFT) Competencies: * Ability to understand the unmet needs of key stakeholders, make decisions that have an impact and execute the integration and assimilation of that information into the IFTs’ engagement approach. * Ability to coordinate scientific/medical engagement efforts across stakeholders within a single account, to develop interaction plans that are inline with the Scientific Interaction Plan (SIP) to achieve medical objectives. * In-depth understanding and execution of meaningful strategies and data-based business decisions to exceed IFT business goals. * Effectively communicate, collaborate, and incorporate the views of other in-field team members to optimize business objectives.      AbbVie is an equal opportunity employer and encourages women, Aboriginal people, persons with disabilities and members of visible minorities to apply.Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html

Medical Science Liaison, Rheumatology, Alberta & B.C. - AbbVie

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Joining AbbVie means, you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada whereby 90% of our employees are proud to say they work for AbbVie and 88% are proud of how we contribute to the community.&lt;br&gt;&lt;br&gt;AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio.&lt;br&gt;&lt;br&gt;When choosing your career path, choose to be remarkable.&lt;br&gt;&lt;br&gt;We have a new opportunity for a Medical Science Liaison (MSL) to join our Medical Affairs team. In this exciting career opportunity, you will develop and nurture relationships, as well as advance our scientific credibility with established and emerging external experts (EEs). Our MSLs respond to requests by providing key scientific/medical information to external experts and internal stakeholders. This role will cover BC and Alberta.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Key Responsibilities:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Develop/maintain key scientific knowledge that enables credible dissemination of information to external experts (EEs) and other healthcare professionals (HCPs), to help the development of professional working relationships.&lt;/li&gt;&lt;li&gt;Participate and follow-up on assigned investigator-initiated studies (IIS), clinical studies and medical projects initiated within the relevant therapeutic area (TA).&lt;/li&gt;&lt;li&gt;Provide scientific support and help maintain relationships with external experts/academic centers.&lt;/li&gt;&lt;li&gt;Deliver credible presentations on scientific matters to HCPs, individually or in groups.&lt;/li&gt;&lt;li&gt;Participate in the selection process to identify qualified HCPs AbbVie would wish to engage in collaborative efforts – such as research, or lecture/meeting support (advisory boards, congresses, symposiums, etc.); and to ensure a high level of scientific or educational integrity in these collaborative efforts.&lt;/li&gt;&lt;li&gt;Attend relevant scientific meetings/conferences and develop summaries of key data presented. &lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Education/Experience Required:&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Doctorate or MD or MSc degree in scientific related discipline and demonstrated experience.&lt;/li&gt;&lt;li&gt;Relevant business experience with solid knowledge of the biotech/pharmaceutical industry.&lt;/li&gt;&lt;ul&gt;&lt;li&gt;Previous experience as an MSL preferred.Relevant. Previous experience in a customer-facing role in the healthcare industry.Experience in the presentation and/or interpretation of scientific or clinical research publications.&lt;/li&gt;&lt;/ul&gt;&lt;li&gt;Knowledge of scientific methods applied to clinical research and the current legislative/regulatory controls.&lt;/li&gt;&lt;li&gt;Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and medical research in general.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Essential Skills &amp;amp; Abilities:&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;English language proficiency (oral and written).&lt;/li&gt;&lt;li&gt;Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)&lt;/li&gt;&lt;li&gt;Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).&lt;/li&gt;&lt;li&gt;Travel required about 30% of the time.&lt;/li&gt;&lt;li&gt;Valid driver’s license and passport.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Key in-Field Team (IFT) Competencies:&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Ability to understand the unmet needs of key stakeholders, make decisions that have an impact and execute the integration and assimilation of that information into the IFTs’ engagement approach.&lt;/li&gt;&lt;li&gt;Ability to coordinate scientific/medical engagement efforts across stakeholders within a single account, to develop interaction plans that are inline with the Scientific Interaction Plan (SIP) to achieve medical objectives.&lt;/li&gt;&lt;li&gt;In-depth understanding and execution of meaningful strategies and data-based business decisions to exceed IFT business goals.&lt;/li&gt;&lt;li&gt;Effectively communicate, collaborate, and incorporate the views of other in-field team members to optimize business objectives.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;AbbVie is an equal opportunity employer and encourages women, Aboriginal people, persons with disabilities and members of visible minorities to apply.&lt;br&gt;&lt;br&gt;Additional Information&lt;br&gt;&lt;br&gt;AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:&lt;br&gt;&lt;br&gt;https://www.abbvie.com/join-us/reasonable-accommodations.html

Medical Science Liaison, Rheumatology, Alberta &amp; B.C.

Medical Science Liaison, Rheumatology, Alberta & B.C.

You need a relevant degree, 2+ years in Oncology, knowledge of clinical trial regulations, strong organizational and communication skills, and demonstrated ethics and integrity.

You will monitor clinical sites, ensure compliance with protocols and regulations, conduct site visits, manage data quality, train site personnel, and negotiate investigator agreements.

Madrid

<div>
 Company Description
 AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
 Responsibilities
 <ul>
 <li>Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.</li>
 <li>Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-3 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.</li>
 <li>Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.</li>
 <li>Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.</li>
 <li>Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.</li>
 <li>Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.</li>
 <li>Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.</li>
 <li>Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.</li>
 </ul> Qualifications 
 <ul>
 <li>Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.</li>
 <li>Minimum of 2 year of clinically-related experience in Oncology.</li>
 <li>Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.</li>
 <li>Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.</li>
 <li>Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.</li>
 <li>Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.</li>
 <li>Demonstrated business ethics and integrity.</li>
 </ul> Additional Information
 <div></div>
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html
</div>


 Company Description
  AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
  Responsibilities
 
  Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
  Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-3 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
  Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
  Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
  Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
  Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
  Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
  Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.
   Qualifications
 
  Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
  Minimum of 2 year of clinically-related experience in Oncology.
  Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
  Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
  Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
  Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
  Demonstrated business ethics and integrity.
   Additional Information
 
  AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
 US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 https://www.abbvie.com/join-us/reasonable-accommodations.html


AbbVie

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