Clinical Safety Lead for Trials & Pharmacovigilance

BioNTech; Greater London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading biotechnology company is seeking a Clinical Safety Manager in London to oversee clinical safety and pharmacovigilance activities across trials. Candidates should have an advanced degree and a minimum of 3 years of experience in clinical research, with strong knowledge of GCP and GVP. The role offers flexible hours and a supportive work culture, contributing to the development of innovative therapies. Apply now to become part of a mission that improves health outcomes worldwide.

Benefits

Flexible hours

Company bike

Employer-funded pension

Childcare

Qualifications

• Advanced degree in life sciences, pharmacy, public health, or related field (PhD preferred).
• Minimum 3 years of clinical research and pharmacovigilance experience, including 2 years of case processing.
• Strong knowledge of GCP, GVP, and regulatory requirements.

Responsibilities

• Lead safety planning and operational set‐up for clinical trials.
• Act as the primary safety contact for assigned trials.
• Supervise end‐to‐end ICSR processes.
• Coordinate SUSAR reporting to regulatory authorities.
• Develop and review safety documents.

Skills

Expertise in clinical safety

Regulatory knowledge

Project management

Scientific writing

Collaboration skills

Fluent English

Education

Advanced degree in life sciences, pharmacy, or public health

Job description

A leading biotechnology company is seeking a Clinical Safety Manager in London to oversee clinical safety and pharmacovigilance activities across trials. Candidates should have an advanced degree and a minimum of 3 years of experience in clinical research, with strong knowledge of GCP and GVP. The role offers flexible hours and a supportive work culture, contributing to the development of innovative therapies. Apply now to become part of a mission that improves health outcomes worldwide.