Clinical Research Coordinator II

Tekton Research Inc•Wichita, KS

14h

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. 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.

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, advanced training preferred

Nice To Haves

advanced training

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
Train and guide CRC I 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