Clinical Research Coordinator
CellmigBiolabs · Raleigh-Durham-Chapel Hill Area · Today
AnalystFull-time
Roles and Responsibilities
- Participate preparation and control of research budgets, timelines, and financial payments
- Manage necessary records of study related activity which includes case report forms
- Keep track of study activities to ensure compliance with protocols and with all related local, state, and national regulatory and institutional policies
- Communicate with clinics and laboratories
- Track all research expenses for clinical studies
- Direct the request, collection, labelling, storage, or shipment of samples
- Perform specific protocol procedures (interviewing patients, collection of samples)
- Compile clinical study data and analyses
- Monitor compliance with protocols and clinical objectives with all relevant regulators
- Participate in the development of protocols and FDA submissions
Requirements
- Bachelor’s degree or more in a life sciences field
- Meticulously organized
- Excellent communication skills to interface with patients, clinicians, regulators, monitors
- Ability to communicate results and concepts clearly to laypeople
- Empathetic “bedside manner”
- Ability to interface on a conceptual level with biology researchers and software engineers
- Exceptional time management
- Able to efficiently find creative solutions to problems
Nice-to-haves
- Clinical research experience
- Good Clinical Practice (GCP) training
- Experience developing standard operating procedures (SOPs)
- Experience working with a licensed IRB and the FDA
- USA citizen only
Benefits
Cellmig offers a competitive salary and benefits.