Hobson Prior is currently seeking a PV Physician (Director Level) for a remote position located in either London or Paris. The successful candidate will be responsible for providing medical and scientific support to pharmacovigilance in accordance with applicable regulatory guidelines/requirements and company Standard Operating Procedures (SOPs).

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities

• In this role, you will oversee and medically assess individual safety case reports.
• Examine all Serious Adverse Events (SAEs) and potentially reportable cases such as SUSARs/INDSRs.
• Maintain close communication with clinical development physicians to ensure availability of essential safety, clinical, and laboratory data.
• Participate in monthly Safety Management Team meetings led by clinical development.
• Chair Safety Review Teams (SRT) for developmental clinical assets.
• Deliver presentations at Joint Safety Review Team meetings.
• Actively engage in monthly Product Development Team meetings and Clinical (study) sub-team meetings.
• Support the signal management process and the identification/assessment of trends and safety signals from various sources.
• Drive proactive implementation of risk management strategies in alignment with global regulatory standards.
• Evaluate critical project documents from a safety standpoint across all projects.
• Offer medical advice and training to pharmacovigilance team members on medical/clinical safety matters.
• Stay updated on safety-related regulations and guidelines.
• Participate in and provide support during Regulatory Authority inspections and audits.

Requirements

• Hold a University Degree in Medicine and Surgery.
• Possess a minimum of eight years' clinical research experience within the pharmaceutical industry.
• Demonstrated experience as a Pharmacovigilance / Drug Safety Physician.
• Demonstrate direct involvement with oncology and small molecule drugs, which is highly advantageous.
• Exhibit thorough knowledge of safety regulations in both EU and US contexts.
• Display a strong grasp of GxP guidelines pertaining to drug safety.
• Demonstrate a proven capacity to work autonomously while effectively prioritizing tasks, with a collaborative spirit and commitment to compliance.
• Showcase exceptional organizational abilities and adeptness at managing multiple competing priorities within tight deadlines.
• Possess outstanding presentation and communication skills.
• Have a solid understanding of standard computer systems; familiarity with ARGUS is a plus.
• Essential fluency in both spoken and written English.
• Be willing and able to travel domestically and internationally.

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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