Clinical Development Medical Director

SRG
London
10 months ago
Applications closed

Related Jobs

View all jobs

Clinical Development Medical Director- Hepatology

GSK Stevenage, United Kingdom
US$202,500 – US$371,250 pa Hybrid

Clinical Development Medical Director - Cardiovascular

GSK Stevenage, United Kingdom
Hybrid

Clinical Development Medical Director- Hepatology

GSK
£202,500 – £371,250 pa Hybrid

Clinical Development Medical Director- Hepatology

GSK United Kingdom
US$202,500 – US$337,500 pa Hybrid

Clinical Development Medical Director- Hepatology

GSK

Clinical Development Medical Director - Cardiovascular

GSK United Kingdom
£222,750 – £371,250 pa
Posted
7 Nov 2025 (10 months ago)

Clinical Development Medical Director

Contract Type: Temporary
Duration: 12 months
Rate: £(Apply online only) per day approx. (Umbrella)

We are closely collaborating with a top global pharmaceutical company, supporting their search for a Clinical Development Medical Director that is needed within their team. This 12 month contract is suited exclusively to physicians in the pharmaceutical industry with experience in Neurology/Neuroscience Clinical Trials.
You will be responsible for leading global clinical strategy and execution for key development programs. You will provide medical oversight, drive regulatory submissions, and collaborate with cross-functional teams to bring innovative therapies to patients worldwide.

Key Responsibilities

Lead clinical strategy and deliverables across assigned programs and trials
Develop and review clinical sections of regulatory documents and submissions
Provide medical oversight and act as medical monitor for clinical trials
Ensure safety monitoring and benefit-risk assessments in collaboration with Patient Safety
Represent the company in interactions with regulatory authorities, KOLs, and advisory boards
Contribute to internal training, mentoring, and global clinical initiatives

Requirements & Experience

MD or equivalent medical degree with ≥4 years clinical practice experience
≥5 years in clinical research or global drug development (Phases I-IV) in pharma or CRO settings
Strong scientific acumen and therapeutic area expertise needed - WITHIN NEUROSCIENCE
Proven ability to lead in a global matrix environment; people management experience preferred
Deep knowledge of ICH-GCP, clinical trial design, and regulatory processes
Excellent communication, interpersonal, and conflict resolution skills

To Apply

If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.