What are the responsibilities and job description for the Unblinded Clinical Research Coordinator position at Tekton Research Inc?
The Unblinded Clinical Research Coordinator supports the daily operations of assigned clinical trials. It is the responsibility of the Unblinded CRC to communicate with CRC II or CRC III, site manager and study participants regarding necessary information of the study. Adherence to site SOPs is required. When working in an Unblinded capacity, the Unblinded CRC’s primary role is managing the Investigational Product (IP) for clinical research trials. This includes, but is not limited to, the receipt, storage, dispensing, destruction, return and administration of IP. The Unblinded CRC is responsible for maintaining the blind of the study for trials required to have blinded and unblinded staff roles. The Unblinded CRC must be the expert on all aspects of IP management for each study they are responsible for. The Unblinded CRC will quickly problem solve issues that may arise with IP management, including reporting dosing discrepancies, ordering issues, and storage excursions.
Essential Qualifications:
- 6 months Clinical Research Coordinator experience, preferred
- Phlebotomy, Vitals, IP Management, Administration & Accountability, required
- Unblinded and/or Pharmacy Technician experience preferred
- Ability to work independently and as a member of a team
- Some college or advanced training/certifications preferred
Tekton Research is a growth-oriented research company focused on excellent conduct of clinical trials. We are team-oriented and core value-centric. We value Focus, Discipline, and Accountability. We offer benefits and a competitive salary. At Tekton Research, we do excellent work and are Making Life Better.
https://tektonresearch.com/
