Senior Pharmacovigilance Physician

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially 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 becoming one of the global leaders in its fields. We cover all therapy areas including medical devices.

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

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs, writing and / or reviewing signal detection reports, writing and / or reviewing aggregate reports (DSURS, PSURS, PBRERs, PADERS), reviewing risk management reports (RMPs) and mentoring junior PV Physicians. The Senior PV Physician I is also expected to support the QPPV in medical aspects and safety issues as may be required by Company or Client.

For the Client

• To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports 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 complete the adverse event tracker for all ICSRs reports.
• To act as a Qualified Person for Pharmacovigilance or support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues.
• To review and approve 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.
• To cooperate in the preparation of and provide input in Risk Management Plans.
• Supporting / to lead the preparation of responses to regulatory authority requests.
• Can act as EEA QPPV and / or Deputy for up to 2 clients if required.
• To review and provide input in Periodic Safety Update Reports, Development Safety Update Reports, ACOs or Annual Safety Reports.
• To act as Company Lead in a specific pharmacovigilance area requiring medical input (e.g. for preparation of reference safety information – Company Core Data Sheet).
• Actively participate in the Drug Safety Review Committee - signal detection and risk evaluation process for Client company medicinal products in the product's life cycle. Serves on Client’s advisory and scientific committees.

Signalling

For the Company

Qualifications

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 :

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!

Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application.

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