Senior clinical data manager.

For our client,an international company working in medical devices,we are looking for a

Senior clinical data manager

Permanent contract

Location: Geneva area

 The Senior Clinical Data Manager will oversee all aspects of the clinical trial data management of the company’s clinical studies conducted in-house and outsourced.

 

Your responsibilities:

• Lead and oversee clinical study Data Management activities conducted in-house and outsourced.

• Oversee EDC vendors, EDC build and performance (e.g. User Acceptance Testing, eCRF edit checks, issue management, EDC supplier management)

• Design CRFs compatible with EDC and paper studies, with the Project Manager and team and ensure data consistency across studies.

• Write or review data management documentation.

• Identify and troubleshoot data management issues and obstacles for studies

• Liaise closely with study statisticians and conduct any necessary QC on data outputs from statisticians.

• Review protocols, Statistical Analysis Plans, CSRs, and other documents as required.

• Development and maintenance of data management SOPs and Work Instructions

 

Your profile: 

• 5+ years of experience in clinical data management /programming in the medical device /pharmaceutical industry.

• Expert in Excel and basics SAS programming skills

• Ability to work in English (daily working language), French would be an asset

• Bachelor’s degree or equivalent in a Life Sciences, Data Management, BioStatistics, or equivalent.

• Capacity to work with a team.

• Proactive and accountable work ethic and ability to multitask.

• Strong organization and detail oriented.