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 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
