Clinical Development

Clinical development professionals are responsible for designing, managing and executing clinical trials that bring new drugs and medical devices to market. This includes everything from protocol development to trial oversight and regulatory submission.

Clinical development roles are found across pharmaceuticals, biotechnology, medical devices and contract research organisations (CROs). Each offers unique opportunities depending on your experience and interests.

Most roles require a degree in life sciences, medicine, nursing or pharmacy. Experience in good clinical practice (GCP) regulated environments, therapeutic area knowledge and trial phase expertise are highly valued. Senior roles may require postgraduate qualifications or specialised certifications.

Yes. We offer both interim and permanent opportunities across the UK, Europe and the US, tailored to your career goals and availability.

Absolutely. Our clinical team includes consultants with deep knowledge of trial phases, therapeutic areas and regional regulations. You’ll be supported by someone who understands your discipline and can match your experience to the right opportunity.

We do. You’ll receive tailored interview preparation, insights into the hiring company and advice on how to present your clinical experience effectively. We help you navigate each step with confidence and clarity.

Some roles may involve travel, especially those related to site monitoring or global trial oversight. However, many positions offer remote or hybrid flexibility depending on the organisation.