Clinical Trials Practitioner-Part time | Hillingdon Hospitals NHS Foundation Trust

Are you passionate about advancing healthcare and making a real impact on patient outcomes? Do you thrive in fast‑paced, innovative environments where no two days are the same? If so, we’d love to hear from you!

We are seeking an enthusiastic and motivated Clinical Trials Practitioner (CTP) to join our vibrant Research & Innovation team, with a specialist focus on Respiratory clinical studies. This is an exciting opportunity to play a key role in delivering high‑quality research that shapes the future of respiratory care.

This part‑time, fixed‑term position (10 months) has been created to support two new commercial Respiratory trials due to open within the Trust, as well as to help address existing backlog. The post holder will work flexibly across Research Operations and Research Delivery, providing essential support as required. Experience in clinical research or Respiratory services is essential, alongside the ability to prioritise workloads and maintain meticulous documentation.

• Work autonomously to manage participants in a portfolio of clinical research studies, ensuring that any research undertaken safeguards the psychological and physical wellbeing of the patients and is conducted according to Good Clinical Practice (GCP) and the Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006.
• Have duty of care in supporting patients and their families throughout participation in research, acting as the participant's advocate at all times.
• Coordinate care of patients on trials, including collection of data and collection and preparation of biological samples in accordance with local, national and international legislation.
• Identify suitable patients for clinical trials, assess their suitability, and ensure informed consent is obtained as per protocol and local guidelines.
• Coordinate the logistics for patient visits and undertake patient assessments in accordance with study protocol.
• Record all data, including adverse and serious adverse events, in accordance with ICH‑GCP.

• Essential experience in clinical research or Respiratory services.
• Ability to prioritise workloads and maintain meticulous documentation.
• Knowledge of Good Clinical Practice (GCP) and Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006.
• Understanding of ICH‑GCP and relevant local, national, and international legislation.
• Strong organisational and communication skills, with a patient‑centred approach.

The postholder will be assisting with Respiratory studies primarily but will also be expected to provide cross‑cover as required.

Part‑time, fixed‑term (10 months), flexible across Research Operations and Research Delivery. This.