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 standardsSkills & 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
Salary description
£350.00 - £500.00 per day