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.
…