Barrington James
Interim Associate director of Drug Safety
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Interim Associate Director of Drug Safety
I am partnered with a leading Biopharmaceutical company who have a strong commitment to innovation and a wide variety of therapeutic areas who are looking to add an experienced and strategically thinking associate director to their expanding team.
Remote Work structure
Competitive pay rate
12 Month contract
Full time
In this role as an associate director of drug safety, you will provide safety oversight, monitor the drug lifecycle from early stages of development through to post marketing, lead post market safety work, case reporting, aggregate reporting and prepare and maintain risk management documents. This role is vital to people who want to maintain high-quality Pharmacovigilance standards and people with an eager attitude to patient safety.
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Key Responsibilities
- Oversee drug safety activities across the product lifecycle.
- Lead safety reviews, signal detection, and risk assessments.
- Manage safety reports and regulatory documents.
- Support benefit-risk decisions and risk management plans.
- Work with global teams to maintain patient safety standards.
Experience you should bring
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- Strong experience in pharmacovigilance and drug safety within the pharmaceutical industry.
- Knowledge of GxP, regulatory requirements, and clinical trial processes.
- Experience with signal detection, safety reporting, and benefit-risk assessments.
- Ability to analyse safety data and communicate findings clearly.
- A life sciences degree (MSc, PhD, Medical or PharmD preferred) with experience working in global teams.
If this role sounds like it’s for you…Apply now
For further information/questions please message me via LinkedIn
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