Clinical Data Coordinator
About the role
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.
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.
- Cookordinate 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.
Requirements
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.
Qualifications
- Bachelor’s degree or equivalent experience in lieu of degree.
- Experience working within a clinical research organization.
Skills
Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable.
Benefits
We value our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
- 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
Pay
Pay Range: $24.00 to $29.00 per hour, based on experience, qualifications, and internal equity.
Schedule
Work Schedule: 8:00 am-5:00 pm EST, Monday-Friday
Location
Location: 629 Cranbury Rd., Suite 102, East Brunswick, NJ 08816