Associate Medical Director – Clinical Development

Associate Medical Director – Clinical Development

Help shape the clinical development of diagnostic radiopharmaceuticals by providing medical and scientific leadership across Phase I-IV studies. This role offers the opportunity to take strategic responsibility for assigned assets while working with experienced cross-functional teams.

Overview

You will be accountable for medical integrity, participant safety and clinically robust study execution from protocol development through close-out. You will work closely with Clinical Operations, Imaging, Biometrics, Pharmacovigilance, Regulatory, Quality and CMC colleagues.

Key Responsibilities

• Provide medical direction for global clinical development activities.

• Develop and review protocols, Investigator Brochures, monitoring plans, clinical study reports and regulatory documentation.

• Act as medical monitor for insourced studies and oversee outsourced medical monitoring.

• Review participant-level medical decisions, safety data, emerging trends and potential signals.

• Lead medical data reviews, clinical query strategies and readiness for database lock.

• Interpret study results and contribute to regulatory submissions, publications, congress materials and development decisions.

• Build effective relationships with investigators, key opinion leaders and clinical sites.

• Support feasibility, recruitment, investigator meetings and advisory activities.

• Identify and resolve study risks, communicate recommendations and maintain inspection readiness.

Must-Have

• MD or equivalent first medical degree, with postgraduate clinical training and/or relevant specialty certification.

• Current or recent registration with the UK General Medical Council, an EU or US equivalent, or eligibility for registration.

• Clinical experience beyond medical-degree training.

• Working knowledge of clinical development, Good Clinical Practice, protocol design, safety surveillance and pharmacovigilance.

• Ability to interpret clinical data, manage priorities and communicate effectively across teams.

Nice-to-Have

• Experience in oncology, radiology, nuclear medicine, pharmaceutical medicine or a related specialty.

• Pharmaceutical or biotechnology experience.

• Higher research degree or formal training in clinical research or drug development.

• Scientific or medical presentation and publication experience.

Travel of up to 20% may be required. Apply to contribute to the development of innovative clinical programmes.