A strong opportunity for an early-career professional to gain hands-on experience across clinical investigations, investigator-initiated studies (IIS), pilot studies, and post-market clinical follow-up.
Key responsibilities:
Support planning and execution of clinical studies across EMEA
Track study progress, data collection, and timelines
Work with investigators and Key Opinion Leaders
Contribute to clinical documentation and evidence generation
Assist with PMCF, PMS, and cross-functional project coordination
Requirements:
Degree in Life Sciences or related field
Understanding of clinical trials and GCP
Strong organisational and communication skills
Willingness to travel (good access to motorways/airports required)
Experience in clinical research or medical devices is advantageous. This role may suit candidates with a Masters in Clinical Trials and some relevant experience, or research nurses within clinical trials units looking to move into industry.
UK location flexible, with travel across EMEA
Salary description
£40000.00 - £45000.00 per year