Global Safety Physician / Deputy QPPV
- Posted 16 October 2024
- LocationUnited Kingdom
- Job type Permanent
- Discipline Medical & Drug Safety
- Reference205402
- Contact NameDominic Pritchard
Job description
BioTalent is collaborating with a well respected Big Pharma to appoint a Global Safety Physician (Deputy QPPV) in a team expansion program. This is a remote based opportunity for EU citizens/residents who have 10+ years experience at a global level + have held QPPV responsibilities before.
Job Title: Global Safety Physician (Deputy QPPV)
Location: Remote (European Union) with business travel (10%)
Position Overview:
We are seeking a highly skilled and motivated Global Safety Physician to join our team. In this role, you will play a crucial part in ensuring the safety and efficacy of our products in both clinical and post-marketing settings. You will also serve as the Deputy Qualified Person for Pharmacovigilance (QPPV), supporting our global pharmacovigilance activities.
Key Responsibilities:
- Lead and oversee safety assessments for clinical trials and post-marketing products.
- Collaborate with cross-functional teams to evaluate and communicate safety profiles of our products.
- Contribute to the development and implementation of risk management strategies.
- Support the QPPV in ensuring compliance with regulatory requirements and pharmacovigilance best practices.
- Participate in the preparation of safety reports and presentations for regulatory authorities and internal stakeholders.
- Mentor and support junior safety staff in their professional development.
Qualifications:
- Medical degree (MD) or equivalent, with relevant board certification preferred.
- Minimum of 10 years of experience in pharmacovigilance or drug safety, with a strong background in both clinical and post-marketing settings.
- Experience in a medium to large-sized pharmaceutical company is highly desirable.
- Strong understanding of regulatory requirements related to pharmacovigilance in the EU (FDA is a bonus).
- Excellent communication skills and ability to work collaboratively in a multidisciplinary team.
- Fluency in English; proficiency in additional European languages is a plus.
Application Process:
If you are passionate about drug safety and are ready to take on this exciting opportunity, please submit your CV to dominic.pritchard@biotalent.ch +41415625046