Data Management Specialist
Job Summary
Providing data management support for Investigator Initiated Trials, the full-time Data Management Specialist will utilize OnCore to build protocol calendar specifications and develop electronic case report forms while collaborating with various protocol staff in a hybrid work environment.
Key responsibilities
- Manage data collection processes throughout the study life cycle
- Develop and implement electronic case report forms (eCRFs) using OnCore
- Collaborate with Principal Investigators, Clinical Research Associates, and other stakeholders on data management tasks
Required qualifications
- Bachelor's degree in a relevant field
- At least 3 years of related experience in data management or clinical trials
- Knowledge of clinical trial design and data management processes
- Experience with electronic data capture (EDC) systems
- Ability to work flexible hours, including some evenings and weekends as needed
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