Clinical Data Coordinator
About The Position
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe. We are hiring a motivated Clinical Data Coordinator who will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies. This position is offered at a pay range of $24.00 to $29.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings. Work Schedule: 8:00 am-5:00 pm EST, Monday-Friday Location: 629 Cranbury Rd., Suite 102, East Brunswick, NJ 08816
Requirements
- High School Diploma/GED.
- 2 years of clinical data entry experience.
- Knowledge and training in general office administration skills, including computer applications, filing system
Nice To Haves
- Bachelor’s degree.
- Ability to accurately perform data review and CRF completion in its entirety with minimal direction.
- Familiarity with medical terminology.
- CCRP or CCRC credentials.
Responsibilities
- Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
- Receive and request patient records/data from the study team as required to complete CRFs for assigned studies.
- Review patient data for completeness and accuracy for assigned studies.
- Coordinate and schedule monitor visits for assigned studies. This includes exit meetings with monitors to review data or queries.
- Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
- Review and utilize protocols as guides for study activities for assigned studies.
- Assure that data entry remains current for all assigned studies.
- Attend meetings as required for assigned studies. This includes, but is not limited to, site initiation meetings, monitor exit meetings, close-out visit meetings, and audit preparation meetings.
- Communicate as needed with accounts receivable staff regarding submitted data.
Benefits
- Comprehensive health coverage: Medical, dental, and vision insurance provided
- Robust retirement planning: 401(k) plan available with employer matching
- Financial security: Life and disability insurance for added protection
- Flexible financial options: Health savings and flexible spending accounts offered
- Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
