Clinical Research Coordinator II
About The Position
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.
Requirements
- 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
Nice To Haves
- advanced training preferred
Responsibilities
- Daily operations and overall management of assigned clinical trials
- Administrative duties
- Regulatory functions
- Clear and direct communication with study sponsor, study monitor, CRO, PI and site management
- Adherence to Tekton SOPs
- Collaborate with CRC I to train and guide them on Tekton SOPs, protocol, and regulatory compliance
- Problem solve issues that may arise
- Represent himself/herself and the site in the most professional, ethical and positive manner
Benefits
- competitive salary
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
Number of Employees
11-50 employees
