PRN Data Coordinator
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Job Description
Part-time remote Data Coordinator transcribing clinical-trial source data into accurate Case Report Forms. Supporting document tracking, reconciliation, and Good Clinical Practice compliance at Worldwide Clinical Trials.
Responsibilities:
- Review study protocols for assigned studies
- Ensure source-document data is accurately reflected on electronic or paper Case Report Forms
- Track source documents filed into subject folders
- Assist with reconciliation of study records for archive
- Identify and report problems or potential problems to the supervisor
- Request, schedule, and attend required training
- Work under the general supervision and guidance of the Senior Manager, Study Conduct
Requirements:
- Excellent written and oral communication skills
- Ability to understand complex written and oral instructions
- Basic computer knowledge and applications for business correspondence and electronic Case Report Form data entry
- Strong interpersonal skills
- Excellent attention to detail
- Some knowledge of the clinical research process, including Good Clinical Practices
- Bachelor’s degree or associate degree, preferably in Life Sciences or Health, and/or experience in a phase I clinical environment
- Preferred: Experience or class work in the health field
Benefits:
- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Transparent compensation and pay equity
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