PrimeVigilance, an Ergomed Group company, was established in 2008 by Dr. Miroslav Reljanovic together with co-founder Dr. Elliot Brown. PrimeVigilance oﬀers holistic, top quality, cost-eﬀective, innovative safety services for pharmaceutical, generic and biotechnology companies. Our founders and leaders have an unrivalled reputation in the sector with a network of expert associates across the world. These include former senior regulators and consultants with extensive industry experience, especially with marketed products.

Science & Healthcare

PrimeVigilance

Bringing expertise to deliver medicines our world can trust.

You need a diploma or degree, 3-5 years of administrative experience, strong English communication skills, MS Office proficiency, and a motivated, approachable personality.

You will support office management, maintain supplies, manage repairs and vendor relations, handle mailings, and assist with various administrative tasks and projects as needed.

People, HR & Administration

Facilities Management

Pune

<div>
 Job Description
 CORE RESPONSIBILITIES
 <ul>
 <li>Supports Office Manager in the functional role and responsibilities that includes wide range of tasks from various office support areas including Office Management, Event Management, Facilities and Health and Safety</li>
 <li>Serves as the first point of contact for the local team, provides information and basic administrative solutions, navigates internal or external clients to the respective specialised dpt. and contact</li>
 <li>Maintains office supply inventories, groceries and manages its orders</li>
 <li>Keeps great condition of the office, arranges necessary repairs, and deals with various vendors ensuring the high quality of deliveries</li>
 <li>Registers and distributes incoming and outgoing mailings, visits post office, orders carrier services, travel insurance, taxi etc.</li>
 <li>Provides photocopying and scanning of documents</li>
 <li>Keeps handover protocols, inventories, contact and other databases up to date</li>
 <li>Contributes to wide range of tasks and projects as per line Managers or Country Director direction</li>
 </ul> Qualifications 
 <ul>
 <li>Minimum graduation/ diploma</li>
 <li>Excellent in English communication verbal and written.</li>
 <li>Should have experience of minimum 3-5 years in office administrative activities.</li>
 <li>Proven administrative experience required</li>
 <li>Great interpersonal skills, approachable personality willing to help</li>
 <li>Good entry level written and verbal communication skills</li>
 <li>Fast learner with scheduling, problem-solving skills, self-motivated attitude</li>
 <li>English, both written and verbal at the level allowing to communicate efficiently with the team</li>
 <li>Common literacy at all MS-Office applications including Microsoft Word, desirably Excel, and PowerPoint</li>
 </ul>
</div>


 Job Description
  CORE RESPONSIBILITIES
 
  Supports Office Manager in the functional role and responsibilities that includes wide range of tasks from various office support areas including Office Management, Event Management, Facilities and Health and Safety
  Serves as the first point of contact for the local team, provides information and basic administrative solutions, navigates internal or external clients to the respective specialised dpt. and contact
  Maintains office supply inventories, groceries and manages its orders
  Keeps great condition of the office, arranges necessary repairs, and deals with various vendors ensuring the high quality of deliveries
  Registers and distributes incoming and outgoing mailings, visits post office, orders carrier services, travel insurance, taxi etc.
  Provides photocopying and scanning of documents
  Keeps handover protocols, inventories, contact and other databases up to date
  Contributes to wide range of tasks and projects as per line Managers or Country Director direction
   Qualifications
 
  Minimum graduation/ diploma
  Excellent in English communication verbal and written.
  Should have experience of minimum 3-5 years in office administrative activities.
  Proven administrative experience required
  Great interpersonal skills, approachable personality willing to help
  Good entry level written and verbal communication skills
  Fast learner with scheduling, problem-solving skills, self-motivated attitude
  English, both written and verbal at the level allowing to communicate efficiently with the team
  Common literacy at all MS-Office applications including Microsoft Word, desirably Excel, and PowerPoint
 


Office Support Coordinator - PrimeVigilance

Office Support Coordinator

You should have a life science background, keen to learn about patient safety, and possess strong communication and multitasking skills with advanced English (B2+) abilities.

You will participate in signal detection, review line listings, draft reports, maintain tracking tools, and collaborate with departments to ensure compliance with procedures and regulations.

Research & Development

Healthcare

<div>
 Company Description
 We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
 Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description
 The Benefit/Risk Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (biotechnology, veterinary science etc.). The Benefit/Risk Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.
 If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them
 The Benefit/Risk Associate will be responsible for:
 <ul>
 <li>Participating in signal detection activities including set-up</li>
 <li>Reviewing line listings required for preparation of signal detection report</li>
 <li>Drafting signal detection reports, including quality control</li>
 <li>Record keeping and maintenance of relevant tracking tools</li>
 <li>Working with other company departments to ensure that signal management is conducted in accordance with relevant PrimeVigilance procedures and regulatory requirements</li>
 </ul> Qualifications 
 <ul>
 <li>Life science / bio medical background – healthcare related degree (biotechnology, veterinary science), previous experience is advantage</li>
 <li>People who are excited to learn and contribute to patient safety</li>
 <li>Time and issue management, delegation, organization and multitasking skills with good attention to detail</li>
 <li>Strong interpersonal and communication skills</li>
 <li>Advanced English skills, both verbal and written, at least B2</li>
 </ul> Additional Information
 Why PrimeVigilance?
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
 We offer:
 <ul>
 <li>Training and career development opportunities internally</li>
 <li>Strong emphasis on personal and professional growth</li>
 <li>Friendly, supportive working environment</li>
 <li>Opportunity to work with colleagues based all over the world, with English as the company language</li>
 </ul>
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 <ul>
 <li>Quality</li>
 <li>Integrity &amp; Trust</li>
 <li>Drive &amp; Passion</li>
 <li>Agility &amp; Responsiveness</li>
 <li>Belonging</li>
 <li>Collaborative Partnerships</li>
 </ul>
 We look forward to welcoming your application.
</div>


 Company Description
  We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
 Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description
  The Benefit/Risk Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (biotechnology, veterinary science etc.). The Benefit/Risk Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.
 If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them
  The Benefit/Risk Associate will be responsible for:
 
  Participating in signal detection activities including set-up
  Reviewing line listings required for preparation of signal detection report
  Drafting signal detection reports, including quality control
  Record keeping and maintenance of relevant tracking tools
  Working with other company departments to ensure that signal management is conducted in accordance with relevant PrimeVigilance procedures and regulatory requirements
   Qualifications
 
  Life science / bio medical background – healthcare related degree (biotechnology, veterinary science), previous experience is advantage
  People who are excited to learn and contribute to patient safety
  Time and issue management, delegation, organization and multitasking skills with good attention to detail
  Strong interpersonal and communication skills
  Advanced English skills, both verbal and written, at least B2
   Additional Information
  Why PrimeVigilance?
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
  We offer:
 
  Training and career development opportunities internally
  Strong emphasis on personal and professional growth
  Friendly, supportive working environment
  Opportunity to work with colleagues based all over the world, with English as the company language
 
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 
  Quality
  Integrity & Trust
  Drive & Passion
  Agility & Responsiveness
  Belonging
  Collaborative Partnerships
 
 We look forward to welcoming your application.


Benefit/Risk Associate II - PrimeVigilance

Benefit/Risk Associate II

You must be a qualified physician with pharmacovigilance experience, good at planning, teamwork, and communication. Experience in aggregate reports or signal detection is a plus.

You will review and approve ICSRs and SAE reports, assess safety data, evaluate literature, contribute to safety reports, participate in signal detection, and propose action for identified signals.

Legal

<div>
 Company Description
 We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Job Description
 Responsibilities include:
 <ul>
 <li>To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding, assessment of seriousness, listedness / expectedness and Company causality, as well as writing of Company comment, follow-up questions and Analysis of Similar Events, when required. Including completion of all required supporting documentation such as trackers.</li>
 <li>To review literature screening search strategy</li>
 <li>To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings</li>
 <li>Reviewing database outputs</li>
 <li>To review and provide input in Periodic Safety Update Reports</li>
 <li>To review and provide input in Development Safety Update Reports</li>
 <li>Participating in signal detection activities including meetings and writing signal detection reports</li>
 <li>Proposing a course of action whenever a possible signal is identified</li>
 </ul> Qualifications 
 <ul>
 <li>Medically qualified as a physician with demonstrated experience in Pharmacovigilance</li>
 <li>Any experience in aggregate reports and signal detection is desirable</li>
 <li>Excellent interpersonal skills</li>
 <li>Ability to plan, organise, prioritise and execute multiple tasks</li>
 <li>Ability to work effectively cross culturally and cross functionally and value the importance of teamwork</li>
 <li>Communication skills</li>
 <li>Presentation skills</li>
 </ul> Additional Information
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? Because our people are our greatest strength leading to our continued success on improving the lives of those around us.
 We offer:
 <ul>
 <li>Training and career development opportunities internally</li>
 <li>Strong emphasis on personal and professional growth</li>
 <li>Friendly, supportive working environment</li>
 <li>Opportunity to work with colleagues based all over the world, with English as the company language</li>
 </ul>
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 <ul>
 <li>Quality</li>
 <li>Integrity &amp; Trust</li>
 <li>Drive &amp; Passion</li>
 <li>Agility &amp; Responsiveness</li>
 <li>Belonging</li>
 <li>Collaborative Partnerships</li>
 </ul>
 Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application!
</div>


 Company Description
  We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Job Description
  Responsibilities include:
 
  To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding, assessment of seriousness, listedness / expectedness and Company causality, as well as writing of Company comment, follow-up questions and Analysis of Similar Events, when required. Including completion of all required supporting documentation such as trackers.
  To review literature screening search strategy
  To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings
  Reviewing database outputs
  To review and provide input in Periodic Safety Update Reports
  To review and provide input in Development Safety Update Reports
  Participating in signal detection activities including meetings and writing signal detection reports
  Proposing a course of action whenever a possible signal is identified
   Qualifications
 
  Medically qualified as a physician with demonstrated experience in Pharmacovigilance
  Any experience in aggregate reports and signal detection is desirable
  Excellent interpersonal skills
  Ability to plan, organise, prioritise and execute multiple tasks
  Ability to work effectively cross culturally and cross functionally and value the importance of teamwork
  Communication skills
  Presentation skills
   Additional Information
  We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? Because our people are our greatest strength leading to our continued success on improving the lives of those around us.
  We offer:
 
  Training and career development opportunities internally
  Strong emphasis on personal and professional growth
  Friendly, supportive working environment
  Opportunity to work with colleagues based all over the world, with English as the company language
 
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 
  Quality
  Integrity & Trust
  Drive & Passion
  Agility & Responsiveness
  Belonging
  Collaborative Partnerships
 
 Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application!


Medical Reviewer I - PrimeVigilance

Medical Reviewer I

You should have a life sciences degree, some pharmacovigilance knowledge, strong organizational and management skills, and excellent communication abilities.

You will create, maintain, and review PSMF documents, ensure quality checks, manage updates, attend meetings, train others, and complete tasks assigned by your Line Manager.

<div>
 Company Description
 We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
 Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description
 The position is primarily responsible for the creation, maintenance and review of client Pharmacovigilance System Master Files, in line with global regulations, legislation, PrimeVigilance and Client requirements.
 The position will maintain and manage PSMF for clients, activities will include PSMF:
 <ul>
 <li>Authoring</li>
 <li>Revision</li>
 <li>Quality check review</li>
 <li>Tracking</li>
 </ul>
 <ul>
 <li>Attend regular PSMF meetings with internal employees and Clients.</li>
 <li>Fulfilment of tasks assigned by the Line Manager.</li>
 <li>Provision of training in PSMF area.</li>
 <li>Revision and update of PSMF related quality documents.</li>
 </ul>
 Qualifications 
 <ul>
 <li>Degree qualification preferred, ideally in life sciences - pharmacy, nursing or other healthcare related qualification</li>
 <li>Some experience/knowledge of Pharmacovigilance is required.</li>
 <li>Organisational skills, including attention to detail and multi tasking.</li>
 <li>Management skills, including time and issue management</li>
 <li>Excellent communication skills</li>
 </ul>
 Additional Information
 Why PrimeVigilance
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
 We offer:
 <ul>
 <li>Training and career development opportunities internally</li>
 <li>Strong emphasis on personal and professional growth</li>
 <li>Friendly, supportive working environment</li>
 <li>Opportunity to work with colleagues based all over the world, with English as the company language</li>
 </ul>
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 <ul>
 <li>Quality</li>
 <li>Integrity &amp; Trust</li>
 <li>Drive &amp; Passion</li>
 <li>Agility &amp; Responsiveness</li>
 <li>Belonging</li>
 <li>Collaborative Partnerships</li>
 </ul>
 Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application.
</div>


 Company Description
  We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
 Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description
  The position is primarily responsible for the creation, maintenance and review of client Pharmacovigilance System Master Files, in line with global regulations, legislation, PrimeVigilance and Client requirements.
 The position will maintain and manage PSMF for clients, activities will include PSMF:
 
  Authoring
  Revision
  Quality check review
  Tracking
 
 
  Attend regular PSMF meetings with internal employees and Clients.
  Fulfilment of tasks assigned by the Line Manager.
  Provision of training in PSMF area.
  Revision and update of PSMF related quality documents.
 
  Qualifications
 
  Degree qualification preferred, ideally in life sciences - pharmacy, nursing or other healthcare related qualification
  Some experience/knowledge of Pharmacovigilance is required.
  Organisational skills, including attention to detail and multi tasking.
  Management skills, including time and issue management
  Excellent communication skills
 
  Additional Information
  Why PrimeVigilance
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
  We offer:
 
  Training and career development opportunities internally
  Strong emphasis on personal and professional growth
  Friendly, supportive working environment
  Opportunity to work with colleagues based all over the world, with English as the company language
 
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 
  Quality
  Integrity & Trust
  Drive & Passion
  Agility & Responsiveness
  Belonging
  Collaborative Partnerships
 
 Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application.



Pharmacovigilance Associate (PSMF) - PrimeVigilance

Pharmacovigilance Associate (PSMF)

You need 5-8 years in a life science field, strong multitasking and communication skills, attention to detail, and advanced English (B2+) to contribute to patient safety.

You will participate in signal detection, review line listings, draft reports, ensure quality control, maintain tracking tools, and collaborate with departments to meet procedures and regulations.

Science

<div>
 Company Description
 We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
 Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description
 The Benefit/Risk Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug safety. The Benefit/Risk Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.
 If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them
 The Benefit/Risk Associate will be responsible for:
 <ul>
 <li>Participating in signal detection activities including set-up</li>
 <li>Reviewing line listings required for preparation of signal detection report</li>
 <li>Drafting signal detection reports, including quality control</li>
 <li>Record keeping and maintenance of relevant tracking tools</li>
 <li>Working with other company departments to ensure that signal management is conducted in accordance with relevant PrimeVigilance procedures and regulatory requirements</li>
 </ul> Qualifications 
 <ul>
 <li>5 - 8 years relevant experience would be required.</li>
 <li>Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science).</li>
 <li>People who are excited to learn and contribute to patient safety</li>
 <li>Time and issue management, delegation, organization and multitasking skills with good attention to detail</li>
 <li>Strong interpersonal and communication skills</li>
 <li>Advanced English skills, both verbal and written, at least B2</li>
 </ul> Additional Information
 Why PrimeVigilance?
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
 We offer:
 <ul>
 <li>Training and career development opportunities internally</li>
 <li>Strong emphasis on personal and professional growth</li>
 <li>Friendly, supportive working environment</li>
 <li>Opportunity to work with colleagues based all over the world, with English as the company language</li>
 </ul>
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 <ul>
 <li>Quality</li>
 <li>Integrity &amp; Trust</li>
 <li>Drive &amp; Passion</li>
 <li>Agility &amp; Responsiveness</li>
 <li>Belonging</li>
 <li>Collaborative Partnerships</li>
 </ul>
 We look forward to welcoming your application.
</div>


 Company Description
  We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
 PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
 We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
 Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description
  The Benefit/Risk Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug safety. The Benefit/Risk Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.
 If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them
  The Benefit/Risk Associate will be responsible for:
 
  Participating in signal detection activities including set-up
  Reviewing line listings required for preparation of signal detection report
  Drafting signal detection reports, including quality control
  Record keeping and maintenance of relevant tracking tools
  Working with other company departments to ensure that signal management is conducted in accordance with relevant PrimeVigilance procedures and regulatory requirements
   Qualifications
 
  5 - 8 years relevant experience would be required.
  Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science).
  People who are excited to learn and contribute to patient safety
  Time and issue management, delegation, organization and multitasking skills with good attention to detail
  Strong interpersonal and communication skills
  Advanced English skills, both verbal and written, at least B2
   Additional Information
  Why PrimeVigilance?
 We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
 To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
  We offer:
 
  Training and career development opportunities internally
  Strong emphasis on personal and professional growth
  Friendly, supportive working environment
  Opportunity to work with colleagues based all over the world, with English as the company language
 
 Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
 
  Quality
  Integrity & Trust
  Drive & Passion
  Agility & Responsiveness
  Belonging
  Collaborative Partnerships
 
 We look forward to welcoming your application.


PrimeVigilance

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