Jennifer Grove

Jennifer is a clinical research project manager with over 15 years experience in the pharmaceutical industry.

Her operational experience, covering phases I to IV, has been gained with a range of companies, including both pharma and CRO. Recent positions, reflecting this scope of experience, have included setting up and management of 2 first-in-man studies for a biotech company, monitoring for a large multinational pharmaceutical company and providing GCP/monitoring consultancy for an investigator-led study. The last 4 years prior to freelancing were spent selecting and managing CROs and freelancers to complete a range of projects in Phase I units, culminating in the role of Senior Programme Manager.

Jennifer has now been freelancing for 5 years, continuing to offer operations management, from study start up through to completion. Capabilities include; writing study documentation, including protocols, patient information leaflets and study aids, and writing SOPs; CRO management; review of external department documents, such as data management (validation) plans and reporting & analysis plans; ethics documentation; all aspects of site management from initiation meetings, through monitoring to site close-out.