What are the responsibilities and job description for the Clinical Research Coordinator II position at Tekton Research?
The CRC II is responsible for the daily operations and overall management of assigned clinical trials including administrative duties and regulatory functions. Responsible for clear and direct communication with study sponsor, study monitor, CRO, PI and site management. Adherence to Tekton SOPs is required. The CRC II works collaboratively with the CRC I to train and guide them on Tekton SOPs, protocol, and regulatory compliance. It is the responsibility of the CRC II to problem solve issues that may arise and to represent himself/herself and the site in the most professional, ethical and positive manner.
Required Skills/Abilities:
● 2 years Clinical Research Coordinator experience required
● Phlebotomy, Vitals, EKG experience required
● IP management, accountability & administration experience required
● Ability to work independently and as a member of a team
● Effective verbal and written communication skills
● Ability to read, write, and speak English language
● Knowledge of high-level medical terminology
● GED or HS Diploma required, advanced training preferred
Mon - Fri / 8am - 5pm
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/