Clinical Research Nurse Practitioner

The Nurse Practitioner/Clinical Research Coordinator (CRC) manages the daily operations of clinical trials. It is the responsibility of the CRC to communicate with the investigator, sponsor and study participants all necessary information of the study and to conduct the study in accordance with the protocol. It is the responsibility of the CRC to problem solve issues that may arise and to represent himself/herself and the site in the most professional, ethical and positive manner. Additional responsibilities included for the Nurse Practitioner include serving as sub-Investigator on studies and performing medical assessments on patients when delegated and appropriate.

Essential Qualifications

• Ability to make sound medical judgement in relation to protocols
• Ability assess safety measures in relation to protocols
• Demonstrated strong verbal and written communication skills
• Ability to work as a team member
• Previous Clinical Research experience, preferred
• Current Nurse Practitioner Licensure for the State of Oklahoma, required