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Clincial Research Coordinator

Med Research One


Location:
Florissant, Missouri 63031
Date:
06/08/2017
2017-06-082017-07-08
Job Code:
CRC1
Job Type:
Employee
Job Status:
Full Time
Categories:
  • Clinical Operations
  • Coordinators
Med Research One
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Job Details

Responsible to facilitate overall coordination of  clinical trials by conducting trial activities in collaboration with the Principle Investigator from study start up, patient recruitment, enrollment, and follow-up visits through study closure; playing a critical role in study conduct.

 

Responsible for educating patients and their families on the research protocol, study procedures, study medication or devices, and what each visit will entail and is expected of the patient for the duration of the trial to ensure full understating as a part of the informed consent process.

 

Coordinate and schedule protocol related research procedures, study visits, and follow-up care. Manage patient enrollment visits and follow up visits through obtaining detailed medical histories, health assessments, adverse event assessments and monitoring laboratory and other testing results. Effective collaboration and communication with our treating physicians is crucial to enroll and manage patients care while in the clinical trials.

 

CRC’s must adhere to the approved protocol, understand and follow good clinical practice (GCP), comply with Institutional policies and standard operating procedures, and comply with federal, state and sponsor policies.

 

Great hours and no weekends. 

Great pay with bonus potential

Requirements

Qualifications

  • Current Registered Nurse (RN) license in the state of practice

  • Current CPR certification required

  • Associates Degree in Nursing (A.D.N) from accredited school of nursing required; Bachelor of Science in Nursing (B.S.N) preferred; three-year diploma from accredited diploma program may be substituted for nursing degree

  • Proficient computer skills

  • Excellent interpersonal skills in order for effective physician collaboration, patient retention, and working together with the research team

  • Ability to review electronic medical records for inclusion/exclusion criteria and ongoing patient management as well as skilled multitasking qualities.