Tekton Research Inc is hiring: Clinical Research Coordinator II in Edmond

Benefits

Qualifications

• •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
• •4 more items(s)

Responsibilities

• •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
• •2 more items(s)