Job Details
Tekton Research is looking for an Unblinded Lead Clinical Research Coordinator to join our team in San Antonio, TX.
The Lead Unblinded CRC team member'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 lead unblinded CRC team member is responsible for maintaining the blind of the study for trials required to have blinded and unblinded staff roles. The lead unblinded/pharmacy team member must be the expert on all aspects of IP management for each study they are responsible for. The lead unblinded/pharmacy team member will quickly problem solve issues that may arise with IP management, including reporting dosing discrepancies, ordering issues, and storage excursions.
Essential Qualifications:
- 3+ years Clinical Research Coordinator experience including Unblinded experience
- IP Prep/Administration, Phlebotomy
- Self motivated, attention to detail, team player
- Ability to work independently and as a member of a team
- Strong communication skills
- GCP Certified
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.