Clinical Development Medical Director

SRG; City Of London; On-site; GBP 100,000 - 125,000; Full time

Job summary

A leading pharmaceutical firm is seeking a Clinical Development Medical Director for a 12-month contract. The ideal candidate will have experience in Neuroscience clinical trials and will be responsible for leading clinical strategy, medical oversight, and regulatory submissions. This role requires strong leadership and communication skills, alongside profound knowledge of drug development processes.

Qualifications

• ≥4 years clinical practice experience.
• ≥5 years in clinical research or global drug development.
• Deep knowledge of ICH-GCP, clinical trial design.

Responsibilities

• Lead clinical strategy and deliverables across programs.
• Develop and review clinical sections of regulatory documents.
• Provide medical oversight and act as medical monitor.

Skills

Clinical research

Neurology expertise

Excellent communication skills

Leadership in a global environment

Education

MD or equivalent medical degree

Job description

Clinical Development Medical Director

Contract Type: Temporary, Duration: 12 months, Rate: £700-800 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, providing medical oversight, driving regulatory submissions, and collaborating 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.