Get more replies from employers
Send a job-specific resume in minutes.
Tekton Research in Edmond, Oklahoma is looking for a Clinical Research Coordinator II to oversee daily operations of clinical trials. Responsibilities include managing communications with sponsors, monitors, and site management, while ensuring adherence to SOPs and training CRC I personnel.
The ideal candidate has a minimum of two years of experience in clinical research and must possess skills in phlebotomy and effective communication. We offer competitive salaries and comprehensive benefits in a collaborative work environment.
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.
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.