Data Manager (Clinical Trials)
Data Manager (Clinical Trials)
Medpace
Leuven, Belgium
This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. This role takes on the responsibility as a leader in data management tasks which take place for the entire duration of a clinical trial. The Data Management team works in conjunction with other departments within Medpace to ensure high data quality. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
- Develop and review Data Management procedures for clinical trials with sponsor companies and other departments.
- Lead the design and validation of the CRF specifications and edit checks for the electronic data capture system used for each study.
- Coordinate overall Data Management by serving as primary contact for the sponsor, external data providers, and all project team members.
- Interact with external data providers, and all project team members in the cross functional team.
- Attend bid defence meetings, teleconferences and face to face sponsor meetings as the lead representative from Data Management.
Qualifications
- Bachelor’s Degree in a Science or Mathematics related field with strong Data Management experience in Clinical Trials; OR
- Master’s Degree in a Science or Mathematics related field with good Data Management experience in Clinical Trials.
- Experience operating as primary contact for Data Management activities, including project oversight and direct vendor or client interaction.
- Computer experience with database, spreadsheet, and EDC software (i.e. SAS, Oracle Clinical, and/or Rave preferred).
- Possess an understanding of database structure and processes in data management.
- A basic knowledge of medical terminology is needed, as well as knowledge of clinical research methodologies.
- Solid oral and written English Language communication skills.
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