Director Safety Scientist
Director Safety Scientist
Posted on :
27-06-2025
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1 Vacancy
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Job Description
Job Title: Director Safety Scientist
Location: Welwyn, with Hybrid work
Salary: competitive market salary
Type: Permanent
CK Group are recruiting for a Director Safety Scientist, to join a growing global pharmaceutical company, on a permanent basis, in Welwyn, Hertfordshire, UK.
Director Safety Scientist will require you to:
Further Responsibilities will include:
Your Background:
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 140 666 in all correspondence.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Location: Welwyn, with Hybrid work
Salary: competitive market salary
Type: Permanent
CK Group are recruiting for a Director Safety Scientist, to join a growing global pharmaceutical company, on a permanent basis, in Welwyn, Hertfordshire, UK.
Director Safety Scientist will require you to:
- Provide safety science and pharmacovigilance support across the drug development lifecycle, from early-phase trials to post-marketing.
- Develop and maintain a deep understanding of the safety profile of assigned products or therapy areas.
- Lead and contribute to signal detection and management activities.
- Oversee safety-related documents including CCDS, RMPs, REMS, DSURs, and PBRERs.
- Act as a key safety contributor on study teams and within global regulatory submissions (INDs, NDAs, MAAs, variations, renewals).
Further Responsibilities will include:
- Reviewing and medically assessing individual and aggregate case safety reports.
- Supporting labelling document updates and risk communication strategies.
- Participating in study teams and cross-functional safety discussions, including input on study protocols and post-authorization safety studies (PASS).
- Ensuring compliance with quality systems and applicable global regulations.
Your Background:
- A degree in a healthcare or life sciences discipline is required; a postgraduate qualification (e.g. MSc, PharmD, MD, PhD) is preferred.
- Significant experience in pharmacovigilance, clinical development, or medical affairs within the pharmaceutical industry.
- Strong understanding of GxP standards, global regulatory requirements, and safety reporting frameworks.
- Experience with signal management systems, regulatory safety submissions, and drug safety databases.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 140 666 in all correspondence.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
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