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Data Coordinator
Worldwide Clinical TrialsData Coordinator ensuring data is accurately transcribed into Case Report Forms at Worldwide Clinical Trials. Responsible for data management and adherence to Good Clinical Practice guidelines.
About the role
Key responsibilities & impact- Reviews study protocol for studies assigned
- Ensure data from source documents for the trial are accurately reflected on the Case Report Form
- Keep track of source documents being filed into subject folders
- Assistance with reconciliation of study records for archive
- Identifies problems or potential problems and reports them to his/her supervisor
- Responsible for requesting, scheduling and attending any training required for this position
Requirements
What you’ll need- Bachelor’s degree or associate Degree (preferably in the field of Life Sciences or Health)
- Experience in a phase I clinical environment
- Preferred: Experience or class work in the health field
Benefits
Comp & perks- Competitive benefits package depending on location
- Health insurance
- Retirement plans
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Data Accuracy VerificationStudy Protocol ReviewCase Report Form ManagementRecord Reconciliation
Soft Skills
Problem-SolvingCommunication