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Study Data Manager
Job summary • Study Data Manager required for Global Pharma in Wavre, Belgium • Candidates must speak fluent English • Contract initially for 6 months, contract likely to be extended • Freelancers welcome to apply
Study Data Manager
Study Data Manager required for Global Pharma in Wavre, Belgium
Candidates must speak fluent English and French
Contract initially for 6 months, contract likely to be extended
Freelancers welcome to apply

PW 5589 Project Data Manager / Clinical Data Manager

An excellent opportunity for an experienced Project Data Manager to join a thriving, Global Pharmaceutical organisation. You’ll be responsible for managing multiple projects, including managing the activities of all CROs and minimising risks to the projects. This is a small and dynamic Clinical Team, mostly at senior level, and your communication skills will be second to none.

Data Manager - REAL WORLD DATA (not clinical trials)

This is an office based role in Marlow, ideally full time. The role is PERMANENT. Essentially, the role would involve you working alongside management consultants and study managers and data analysts in the design, development, implementation and data management of Real World Data (observational Data) projects.

Clinical Data Manager (Belgium)

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

Clinical Data Manager – Basel, Switzerland

Clinical Data Manager with leading Swiss firm

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