Responsibilities :
- Effectively plan and execute Data Management projects from study start-up to database lock.
- Serve as a subject matter expert.
- Work directly with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies.
- Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules.
- Communicate with cross-functional groups and stakeholders throughout the project lifecycle.
- Manage sponsor / vendor relationships to ensure efficiency and quality.
- Maintain Quality control of the clinical data, project deliverables, and closeouts.
Requirements :
- Years of Experience as a CDM.
- Excellent organizational and project management skills.
- Technical skills with EDC systems (Medidata Rave, Inform, Medrio, etc.).
- Able to work independently and in teams.
- Excellent organizational and time management skills, with the ability to multi-task.
- Strong interpersonal communication and presentation skills.
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