In a patient centric, fast paced environment, this role is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. Completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. Maintains accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator (CRC) is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.
The successful applicant should have a College degree or be a licensed, clinical professional who understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines. Previous CRC experience may be considered in lieu of this requirement. She/he should be able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner. Should be knowledgeable in medical terminology and demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy. Finally, excellent interpersonal communication skills and the ability to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
Job Type: Full-time
- clinical research: 1 year (Preferred)
- RN, LPN or Paramedic (Preferred)
- Health insurance
- Dental insurance
- Vision insurance
- Retirement plan
- Paid time off
This Company Describes Its Culture as:
- Detail-oriented -- quality and precision-focused
- Outcome-oriented -- results-focused with strong performance culture
- Team-oriented -- cooperative and collaborative