Support the delivery of site activation and maintenance activities for assigned studies or multi-protocol programmes
Job Summary
Support the delivery of site activation and maintenance activities for assigned studies or multi-protocol programmes.
You will help ensure regulatory submissions, contracts, and essential documents are managed compliantly and efficiently, while developing your leadership and project management experience.
This is an excellent opportunity for someone looking to step into greater responsibility within Regulatory & Start‑Up, gain exposure to global studies, and develop leadership capability within a supportive and collaborative clinical research environment.
Matching Summary
Support the delivery of site activation and maintenance activities for assigned studies or multi-protocol programmes.
Skills & Requirements
Must-have
site activation and maintenance
regulatory submissions
contractual documentation
clinical study milestones
GCP, ICH, and applicable regulations
Nice-to-have
leadership capability
complex international studies
proactive, solution-focused mindset
build strong working relationships
Key Requirements
Bachelor’s degree in a related scientific or clinical field
2–3 years’ relevant experience in clinical research
Around 3 years’ clinical research experience
Good knowledge of clinical research processes, medical terminology, and regulations
Experience working with clinical systems and strong Microsoft Office skills
Ability to manage multiple tasks and priorities with attention to detail