Job Description

Clinical Safety Scientist

Type: Temporary
Duration: 6 months initially
Location: London (hybrid working available
Rate: (INSIDE IR35) up to 500 per day (Umbrella)

We are seeking a Safety Scientist to support the safety evaluation and risk management of medicines, with a particular focus on HIV treatments and prevention. This is a critical role contributing to patient safety across the full product lifecycle-from late-stage development through to post-marketing.

Key Responsibilities

• Monitor and evaluate the safety profiles of assigned products across development and post-marketing phases
• Conduct signal detection and evaluation, including analysis of safety data and literature review
• Contribute to the development and maintenance of Risk Management Plans and regulatory safety documentation
• Support preparation of key regulatory deliverables (e.g., DSURs, PBRERs, EU RMPs, licence renewals)
• Collaborate with safety physicians on benefit-risk assessments and individual case safety reviews
• Ensure all safety documentation meets global regulatory and compliance standards

Skills & Experience Required

• Degree (BSc or higher) in Biomedical Sciences, Life Sciences, or related healthcare field
• Proven experience in clinical trial data review and pharmacovigilance activities
• Strong scientific writing skills with experience in regulatory safety documents
• Knowledge of signal detection, causality assessment, and safety data evaluation
• Experience in literature review, data analysis, and interpretation
• Understanding of pharmacovigilance regulations and drug development processes (HIV knowledge advantageous)

To Apply

Please click below and/or to discuss further, contact Theo Charles on (phone number removed)

PAYE also possible - please enquire for more information

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.