Full-Time Senior PV Physician

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, expectedness, and company causality, as well as writing of company comment, follow-up questions and analysis of similar events. This includes completion of all required supporting documentation such as trackers.

To support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues.

To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings Reviewing database outputs.

Requirements:

• Medical qualification as a Physician
• Ability to work effectively cross culturally and value the importance of teamwork
• Presentation skills
• Advanced knowledge of English and MS Office

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.

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

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