Clinical Project Manager

I am currently partnered with a cutting edge organisation that is leading the way within the infectious and respiratory disease area, they are now looking to appoint a Clinical Project Manager to their team within the UK.

The Clinical Project Manager will be responsible for clinical operational oversight as well as the execution of all assigned studies, monitoring of study deliverables, performing protocol-related site management activities, participating in study planning and set-up activities including vendor management, project management, and coordination of study and implementation plans and supporting third party vendor relationships.

 Requirements

• Study set-up and management of global phase I-II studies including study set-up, project management, monitoring, data management, biostatistics and clinical study report
• Site, CRO and vendor management experience
• Evidence & experience of your input into study design
• Writing key study documents contributing to the preparation, design and/or review of essential regulatory study documents, ethics and other required local/national submission requirements
• Demonstrable experience of regulatory and ethics submissions
• Management of study contracts and budgets including maintaining study trackers to provide financial and management accountability
• Pharmacovigilance & Safety monitoring experience
• Data Management and monitoring