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A Global Biotech Organisation in Uxbridge are seeking a Clinical Research Study Manager to work office based on a 12 month contract role.

Contact Deborah Toby at Real Pharma on 0207 758 7322.

Clinical Data Manager (Belgium) Duration: Ongoing contract. The Clinical Data Manager – Data Integration Specialist is a key member of a multidisciplinary team involved in implementing CDISC data standards in clinical trials. As such, you convert legacy (or on-ongoing) clinical study data and metadata into a CDISC format in order to comply with the Food and Drug administration (FDA) submission requirements

inVentiv Health are currently recruiting for an experienced Data Manager for a 12 month contract working on our clients' site in Surrey. Working within a global team, you will primarily be responsible for Data Management activities for the company's consumer health products.

The Project Data Manager (PDM) is responsible for the data management aspects of one or more clinical studies or project. These studies would be like 3 to 4 Phase 2a studies plus 3 Phase I studies.. The PDM will be responsible for the effective communication within the corporation and, where appropriate, with external organisations of the issues and actions related to the successful completion of data management activities within the project(s).

Depending on your current experience level, there is one role available.