Large

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Science & Healthcare

Fortrea

Healthcare

You must prioritize and assign cases, maintain databases, track progress, ensure timely follow-up, reconcile data daily, and support Pharmacovigilance activities as needed.

You will prioritize and assign cases, track progress, update data sheets, reconcile metrics, and support Pharmacovigilance activities to ensure timely case processing and compliance.

Research & Development

Manila

<div><div>As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.</div><ul><li>Segregate cases received as per priority and due dates in the database worklist.</li><li>Assign cases to case processing team based on the priority and availability of resources in consultation with Team Lead or designee.</li><li>Enter data into the Master case tracking sheet. Track and monitor the case progression with help of case tracking sheet. Follow up with associates and/or team leads to ensure timely completion of review and ensure case prioritization.</li><li>Reconciliation of TAT data on a daily basis to ensure all the cases are assigned and reviewed as per SLA.</li><li>Ensure timely updating of productivity, QC and other role specific trackers on a real time basis and follow up with Team Leads for the same.</li><li>Daily reconciliation of received and processed cases to ensure all received cases is processed with internal timelines.</li><li>Perform any other Pharmacovigilance support activities as assigned &ndash; tracking various types of information and metrics, reconciliation of data from multiple sources.</li></ul><div>
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.</div><div></div><div>
Fortrea is proud to be an Equal Opportunity Employer:</div><div><br>
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.</div><div></div><div>
For more information about how we collect and store your personal data, please see our <div>Privacy Statement</div>.</div></div>

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.Segregate cases received as per priority and due dates in the database worklist.Assign cases to case processing team based on the priority and availability of resources in consultation with Team Lead or designee.Enter data into the Master case tracking sheet. Track and monitor the case progression with help of case tracking sheet. Follow up with associates and/or team leads to ensure timely completion of review and ensure case prioritization.Reconciliation of TAT data on a daily basis to ensure all the cases are assigned and reviewed as per SLA.Ensure timely updating of productivity, QC and other role specific trackers on a real time basis and follow up with Team Leads for the same.Daily reconciliation of received and processed cases to ensure all received cases is processed with internal timelines.Perform any other Pharmacovigilance support activities as assigned – tracking various types of information and metrics, reconciliation of data from multiple sources.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.

Assistant Workflow Analyst II - Fortrea

Assistant Workflow Analyst II

You need a degree in life sciences or relevant experience in clinical research. Knowledge of ICH/GCP, drug development, and fluency in English and local language are essential.

You will ensure protocol performance, manage timelines and resources, oversee quality and compliance, collaborate with external partners, and support internal strategy alignment.

Madrid

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div>
  This role is for upcoming future opportunities they may arise at Fortrea
 </div>
 <div>
  The local study manager is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight, and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during the study. Significant impact on the ability to effectively conduct clinical studies and develop the pipeline, while maintaining local regulatory and compliance requirements in countries. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives. As a customer-facing role, this position will build business relationships and represent Client with investigators, functional outsourcing partners and other external partners and therefore have a significant impact on country-level customer relationships. Requires ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, oversight and supervision of the Country Research Director or Therapeutic Director. Requires strong understanding of local regulatory environment, country regulations, client policies and procedures, quality standards. Strong scientific and clinical research knowledge is required for this position. A strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and protocols simultaneously. Requires skills to effectively build and maintain professional relationships with investigators and other external stakeholders, requiring strong communication, educational/pedagogic, diplomatic, and empathic skills. The role will require proven ability to collaborate and lead high performing cross-functional teams also in a virtual environment. The position requires strong leadership skills (scientific and business) and ability to coordinate and lead local teams to high performance. Oversee country commitments, compliance, and training needs. Additionally, business leadership and alignment with corporate requires that individual has ability to lead across several dimensions simultaneously. Works collaboratively with Country and Regional Operations; Pharmacovigilance, Regulatory, Global Medical Affairs and Global Human Health internally; and with external functional outsourcing vendors. Requires coordination and alignment with the regional and broader organization. Additionally, will work to build and maintain relationships with investigators and other external partners and promote Client’s reputation. In collaboration with CRD, represents Client in Pharma industry issues and in seeking influence in external R&amp;D environment.
 </div>
 <div>
  Summary of Responsibilities:
 </div>
 <ul>
  <li>PERFORMANCE: Accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Client policies and procedures, quality standards and adverse event reporting requirements internally and externally. 30%</li>
  <li>MANAGEMENT: POC for assigned protocols. Pro-actively drives/tracks execution and performance of deliverables/timelines/results to meet country commitments for assigned protocols. Strong collaboration with local CO roles. Forecasts country resource needs. Serves local business needs (signs contracts, manages budgets as delegated). 20%</li>
  <li>QUALITY OVERSIGHT: Responsible for quality and compliance in assigned protocols in country. Oversees CRAs and CTCs on assigned projects. Oversees training compliance. Performs quality control visits. Reviews Monitoring Visits Reports and escalates performance issues and training needs to functional vendor and internal management as needed. Oversees associate CRMs assigned to the Client and work on training needs in collaboration with functional vendor. 20%</li>
  <li>EXTERNAL CUSTOMER FACING: Responsible for collaboration with functional outsourcing vendors, investigators, other external partners. Oversees country and site validations, site selection and recruitment in assigned protocols. Responsible for clinical trial education to sites. Country POC for programmatically outsourced trials for assigned protocols. 20%</li>
  <li>INTERNAL COLLABORATION &amp; STRATEGY: Collaborates internally with local PV, Regulatory, GMA/GHH to align on key decisions in countries. Supports local and regional strategy development consistent with long-term corporate needs in conjunction with CRD and Regional Operations. 10%</li>
  <li>All other duties as needed or assigned.</li>
 </ul>
 <div>
  Qualifications (Minimum Required):
 </div>
 <ul>
  <li>University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.</li>
  <li>MANDATORY, In lieu of the above requirement, candidates with minimum of two or more years of relevant clinical research experience as local study manager in pharmaceutical or CRO industries or experience in a health care setting will be considered.</li>
  <li>Fortrea may consider relevant and equivalent experience in lieu of educational requirements.</li>
  <li>Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries.</li>
  <li>Thorough understanding of the drug development process.</li>
  <li>Fluent in local office language and in English, both written and verbal.</li>
 </ul>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
  This role is for upcoming future opportunities they may arise at Fortrea
 
 
  The local study manager is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight, and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during the study. Significant impact on the ability to effectively conduct clinical studies and develop the pipeline, while maintaining local regulatory and compliance requirements in countries. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives. As a customer-facing role, this position will build business relationships and represent Client with investigators, functional outsourcing partners and other external partners and therefore have a significant impact on country-level customer relationships. Requires ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, oversight and supervision of the Country Research Director or Therapeutic Director. Requires strong understanding of local regulatory environment, country regulations, client policies and procedures, quality standards. Strong scientific and clinical research knowledge is required for this position. A strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and protocols simultaneously. Requires skills to effectively build and maintain professional relationships with investigators and other external stakeholders, requiring strong communication, educational/pedagogic, diplomatic, and empathic skills. The role will require proven ability to collaborate and lead high performing cross-functional teams also in a virtual environment. The position requires strong leadership skills (scientific and business) and ability to coordinate and lead local teams to high performance. Oversee country commitments, compliance, and training needs. Additionally, business leadership and alignment with corporate requires that individual has ability to lead across several dimensions simultaneously. Works collaboratively with Country and Regional Operations; Pharmacovigilance, Regulatory, Global Medical Affairs and Global Human Health internally; and with external functional outsourcing vendors. Requires coordination and alignment with the regional and broader organization. Additionally, will work to build and maintain relationships with investigators and other external partners and promote Client’s reputation. In collaboration with CRD, represents Client in Pharma industry issues and in seeking influence in external R&D environment.
 
 
  Summary of Responsibilities:
 
 
  PERFORMANCE: Accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Client policies and procedures, quality standards and adverse event reporting requirements internally and externally. 30%
  MANAGEMENT: POC for assigned protocols. Pro-actively drives/tracks execution and performance of deliverables/timelines/results to meet country commitments for assigned protocols. Strong collaboration with local CO roles. Forecasts country resource needs. Serves local business needs (signs contracts, manages budgets as delegated). 20%
  QUALITY OVERSIGHT: Responsible for quality and compliance in assigned protocols in country. Oversees CRAs and CTCs on assigned projects. Oversees training compliance. Performs quality control visits. Reviews Monitoring Visits Reports and escalates performance issues and training needs to functional vendor and internal management as needed. Oversees associate CRMs assigned to the Client and work on training needs in collaboration with functional vendor. 20%
  EXTERNAL CUSTOMER FACING: Responsible for collaboration with functional outsourcing vendors, investigators, other external partners. Oversees country and site validations, site selection and recruitment in assigned protocols. Responsible for clinical trial education to sites. Country POC for programmatically outsourced trials for assigned protocols. 20%
  INTERNAL COLLABORATION & STRATEGY: Collaborates internally with local PV, Regulatory, GMA/GHH to align on key decisions in countries. Supports local and regional strategy development consistent with long-term corporate needs in conjunction with CRD and Regional Operations. 10%
  All other duties as needed or assigned.
 
 
  Qualifications (Minimum Required):
 
 
  University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
  MANDATORY, In lieu of the above requirement, candidates with minimum of two or more years of relevant clinical research experience as local study manager in pharmaceutical or CRO industries or experience in a health care setting will be considered.
  Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries.
  Thorough understanding of the drug development process.
  Fluent in local office language and in English, both written and verbal.
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Local Study Manager - FSPx Team - Home Based Madrid - Fortrea

Local Study Manager - FSPx Team - Home Based Madrid

You need 0-6 months of call center experience and a healthcare-related bachelor's degree (nursing, pharmacy, medtech, PT, Radtec).

You will respond to medical queries, record adverse reactions, manage drug safety data, support various activities, ensure data quality, and handle additional tasks as assigned.

Customer Relations

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <ul>
  <li>To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.</li>
  <li>Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over telephone calls, email, fax etc.</li>
  <li>Execute drug safety data management processes – a combination of call intake, call dialogue documentation, peer review, case follow-up.</li>
  <li>Perform and support different activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources.</li>
  <li>Assume responsibility for quality of data processed.</li>
  <li>All other duties as needed or assigned.</li>
 </ul>
 <div></div>
 <div>
  Qualifications:
 </div>
 <ul>
  <li>0 to 6 months of call center experience</li>
  <li>Healthcare-related bachelor's degree e.g. nursing, pharmacy, medtech, PT, Radtec</li>
 </ul>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
  To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.
  Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over telephone calls, email, fax etc.
  Execute drug safety data management processes – a combination of call intake, call dialogue documentation, peer review, case follow-up.
  Perform and support different activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources.
  Assume responsibility for quality of data processed.
  All other duties as needed or assigned.
 
 
 
  Qualifications:
 
 
  0 to 6 months of call center experience
  Healthcare-related bachelor's degree e.g. nursing, pharmacy, medtech, PT, Radtec
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Medical Contact Center Assistant I - Fortrea

Medical Contact Center Assistant I

You should be pursuing a degree in a related field, have an interest in Science or Sales, strong communication skills, an analytical mindset, and proficiency in MS Office, especially Excel.

You will assist Inside Sales Managers with prospecting, researching leads, preparing outreach for conferences, and managing essential tools and processes while collaborating with Business Development teams.

Science

Sales & Business Development

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div>
  Fortrea 2025 University Internship Program
 </div>
 <div>
  <br> Inside Sales Team EU
 </div>
 <div>
  <br> Location: UK, remote (occasional travel to Maidenhead)<br> Full-time, 12-month<br> Start Date: July 2025
 </div>
 <div></div>
 <div>
  This program is designed to support your professional development and career exploration through training workshops, leadership speakers, employee resource group activities and career-focused discussions.
 </div>
 <div></div>
 <div>
  Take pride in helping deliver solutions that bring life-changing medicines to patients faster while creating lasting value for all our stakeholders.
 </div>
 <div></div>
 <div>
  About the Team
 </div>
 <div>
  The Inside Sales EU team plays a critical role in identifying new opportunities, building connections, and creating pipelines for business growth. As part of this team, you’ll support Inside Sales Managers by assisting with prospecting, researching potential leads across Europe, preparing outreach for conferences, and managing tools and processes essential to the team's success.
 </div>
 <div>
  This collaborative role allows you to interact with Business Development partners and cross-functional teams, contributing directly to the sales process.
 </div>
 <div></div>
 <div>
  Education/Qualifications/Skills
 </div>
 <ul>
  <li>Working toward a bachelor’s or master’s degree in Life Sciences, Business, Business Management or a related field.</li>
  <li>Interest in Science, Pharma, Clinical Trials, or Sales and Business Development.</li>
  <li>Strong communication and organizational skills, with the ability to collaborate effectively with internal stakeholders.</li>
  <li>Analytical mindset and a proactive approach to problem-solving.</li>
  <li>Proficiency in MS Office tools, particularly Excel.</li>
 </ul>
 <div></div>
 <div>
  We look forward to helping you kickstart your career!
 </div>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
  Fortrea 2025 University Internship Program
 
 
   Inside Sales Team EU
 
 
   Location: UK, remote (occasional travel to Maidenhead) Full-time, 12-month Start Date: July 2025
 
 
 
  This program is designed to support your professional development and career exploration through training workshops, leadership speakers, employee resource group activities and career-focused discussions.
 
 
 
  Take pride in helping deliver solutions that bring life-changing medicines to patients faster while creating lasting value for all our stakeholders.
 
 
 
  About the Team
 
 
  The Inside Sales EU team plays a critical role in identifying new opportunities, building connections, and creating pipelines for business growth. As part of this team, you’ll support Inside Sales Managers by assisting with prospecting, researching potential leads across Europe, preparing outreach for conferences, and managing tools and processes essential to the team's success.
 
 
  This collaborative role allows you to interact with Business Development partners and cross-functional teams, contributing directly to the sales process.
 
 
 
  Education/Qualifications/Skills
 
 
  Working toward a bachelor’s or master’s degree in Life Sciences, Business, Business Management or a related field.
  Interest in Science, Pharma, Clinical Trials, or Sales and Business Development.
  Strong communication and organizational skills, with the ability to collaborate effectively with internal stakeholders.
  Analytical mindset and a proactive approach to problem-solving.
  Proficiency in MS Office tools, particularly Excel.
 
 
 
  We look forward to helping you kickstart your career!
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Inside Sales - 12 month Internship - Start date July 2025 - Remote UK (occasional travel to Maidenhead) - Fortrea

United Kingdom

Inside Sales - 12 month Internship - Start date July 2025 - Remote UK (occasional travel to Maidenhead)

You need a related degree, 2 years of monitoring experience, knowledge of ICH GCP, respiratory/cardiology experience, and fluency in English and local language. Ready for 60% travel.

You will manage sites, conduct monitoring visits, ensure compliance, verify data integrity, oversee regulatory documents, and assist with project administration and training in oncology trials.

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div>
  This role is for upcoming future opportunities that may arise at Fortrea.
 </div>
 <div></div>
 <div>
  Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.<br>
  <ul>
   <li>Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.</li>
   <li>Prepares and implements project plans related to Clinical Monitoring responsibilities.</li>
   <li>Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.</li>
   <li>Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.</li>
   <li>Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.</li>
   <li>Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.</li>
   <li>Ensures adherence to global quality control and CRA performance metrics.</li>
   <li>Ensures audit readiness at site level.</li>
   <li>Acts in the project role of a Lead CRA as assigned.</li>
  </ul>
 </div>
 <div></div>
 <div>
  General On-Site Monitoring Responsibilities:<br>
  <ul>
   <li>Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.</li>
   <li>Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.</li>
   <li>Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.</li>
   <li>Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.</li>
   <li>Travel, including air travel, may be required and is an essential function of the job.</li>
   <li>Prepare and submit accurate and timely trip reports.</li>
   <li>Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.</li>
   <li>Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.</li>
   <li>Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/e-Clinical systems.</li>
   <li>Track IP shipments and supplies, as needed.</li>
   <li>Track and follow-up on serious adverse events as assigned.</li>
   <li>Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.</li>
   <li>Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.</li>
   <li>Attend investigators’ meetings (if applicable), project team meetings and teleconferences, and others as needed.</li>
   <li>Present training content for site initiation.</li>
   <li>Assist with training of new employees (e.g., co-monitoring).</li>
   <li>Perform other duties as assigned by management.</li>
  </ul>
 </div>
 <div></div>
 <div>
  Qualifications (Minimum Required):<br>
  <ul>
   <li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.</li>
   <li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.</li>
  </ul>
 </div>
 <ul>
  <li>Thorough knowledge of monitoring procedures.</li>
  <li>Basic understanding of the clinical trial process.</li>
  <li>Fluent in local office language and in English, both written and verbal.</li>
 </ul>
 <div></div>
 <div>
  Experience (Minimum Required):<br>
  <ul>
   <li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).</li>
  </ul> AND<br>
  <ul>
   <li>A minimum of 2 years of Clinical Monitoring experience.</li>
  </ul>
 </div>
 <ul>
  <li>Respiratory and/or Cardiology Monitoring experience.</li>
 </ul>
 <div></div>
 <div>
  Physical Demands / Work Environment:<br>
  <ul>
   <li>Must be able to sit at a computer for long periods of time.</li>
   <li>Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day.</li>
   <li>Standard office and/or home working environment.</li>
   <li>Clinical Research Unit and hospital environment (administrative only).</li>
   <li>Risk of eye strain.</li>
   <li>Will involve outside of normal office hours as required by the role.</li>
   <li>Travel Requirement is 60% of the time (traveling to study sites)</li>
  </ul>
 </div>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
  This role is for upcoming future opportunities that may arise at Fortrea.
 
 
 
  Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
  
   Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
   Prepares and implements project plans related to Clinical Monitoring responsibilities.
   Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
   Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
   Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.
   Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.
   Ensures adherence to global quality control and CRA performance metrics.
   Ensures audit readiness at site level.
   Acts in the project role of a Lead CRA as assigned.
  
 
 
 
  General On-Site Monitoring Responsibilities:
  
   Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
   Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.
   Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.
   Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
   Travel, including air travel, may be required and is an essential function of the job.
   Prepare and submit accurate and timely trip reports.
   Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.
   Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.
   Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/e-Clinical systems.
   Track IP shipments and supplies, as needed.
   Track and follow-up on serious adverse events as assigned.
   Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.
   Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.
   Attend investigators’ meetings (if applicable), project team meetings and teleconferences, and others as needed.
   Present training content for site initiation.
   Assist with training of new employees (e.g., co-monitoring).
   Perform other duties as assigned by management.
  
 
 
 
  Qualifications (Minimum Required):
  
   University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
   Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
  
 
 
  Thorough knowledge of monitoring procedures.
  Basic understanding of the clinical trial process.
  Fluent in local office language and in English, both written and verbal.
 
 
 
  Experience (Minimum Required):
  
   University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
   AND
  
   A minimum of 2 years of Clinical Monitoring experience.
  
 
 
  Respiratory and/or Cardiology Monitoring experience.
 
 
 
  Physical Demands / Work Environment:
  
   Must be able to sit at a computer for long periods of time.
   Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day.
   Standard office and/or home working environment.
   Clinical Research Unit and hospital environment (administrative only).
   Risk of eye strain.
   Will involve outside of normal office hours as required by the role.
   Travel Requirement is 60% of the time (traveling to study sites)
  
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Fortrea

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