Proclinical Staffing
Associate Safety Director
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Associate Safety Director - Leading Pharma Company
Proclinical is seeking an Associate Safety Director to provide safety science and pharmacovigilance expertise across a diverse portfolio. In this role, you will play a pivotal part in ensuring patient safety by leading safety oversight activities, managing risks, and contributing to both early and late-phase development.
Key Responsibilities
- Provide oversight and input across all stages of study management, from development through post-market.
- Lead post-market safety activities, including signal evaluation, benefit-risk assessments, and safety risk management.
- Manage individual and aggregate case reporting, including key activities such as DSUR and PBRER preparation.
- Drive signal detection and management, contributing to strategic safety assessments and drug safety reports.
- Influence product safety strategies and provide drug safety input into clinical development plans.
- Prepare and maintain safety documents, including CCDS, IB, risk communications, RMP, and REMS.
- Act independently with minimal supervision, demonstrating strong self-leadership and initiative.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Key Requirements
- Advanced degree in life sciences (e.g., PhD, MSc) or a medical qualification (e.g., PharmD) is preferred.
- Extensive & recent, experience in signal detection, aggregate reporting, benefit-risk & DSUR/PBRER's
- Strong understanding of GxP-regulated processes and the clinical trial lifecycle.
- Excellent written and verbal communication skills, with the ability to collaborate effectively with global teams.
- Proficiency in analysing and interpreting complex scientific data, with strong presentation skills.
- Proven ability to work independently, manage safety responsibilities, and support safety science activities.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills