Research & Development Institute, Inc.
  • Thousand Oaks, CA, USA
  • Part Time

Job Description

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration

of clinical trials under the direction of the Study Principal Investigator and Clinical Research Project Manager. The CRC will perform various administrative duties that require good judgment, efficiency, and a high level of experience operating under clinical protocols.

CRC's time will be split between conducting patient visits on-site at the doctor's office and performing administrative and data entry activity at the RDI Facility.

DUTIES AND RESPONSIBILITIES

 

  • Coordinate clinical trials related responsibilities and duties
  • Adhere to Good Clinical Practices, local and national regulations, and the clinical trial protocols
  • Ensure integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
  • Discuss study protocols with patients and collect informed consent documentation
  • Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study
  • Dispense study medication in a professional and accountable manner following protocol requirements
  • Collect, process, and ship blood/urine specimens at scheduled patient visits
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy
  • Ensure that non-serious and serious adverse events are properly documented and reported
  • Screen all laboratory results when received and follow protocol procedure regarding abnormal results
  • Ensure all laboratory results are given to appropriate doctors for review of clinical significance, then file results in the patient study binder
  • Submit patient reimbursement requests at the conclusion of patient's participation in protocol
  • Ensure the filing and maintenance of all regulatory documents
  • Schedule monitor visits and set up for monitoring visits prior to monitor's arrival
  • Other duties as assigned.

 

EDUCATION & EXPERIENCE

 

Associates Degree in Nursing, RN or PA.

Minimum 2 years of experience in a related healthcare position, or equivalent combination of education and experience.

Previous experience with clinical trials preferred

 

 Job Type: Part-time / Contract Basis

 

About RDI

RDI is a trial management organization connecting IVD manufacturers and pharmaceutical companies with a network of doctors participating in advancing medical research.   

We simplify the clinical trial process for Pharmaceutical and Device Sponsors while recruiting, educating, and training independent physicians to participate in pharmaceutical and in-vitro diagnostic studies, unlocking access to valuable patients.      

We recently raised growth capital and are building our business processes and expanding nationwide.

Research & Development Institute, Inc.
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