Clinical Research Coordinator
Novex Clinical Research, LLC - New Bedford, MA

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Clinical Research Coordinator in a multi-specialty privately owned clinical research site. Responsible for the implementation, management, and administration of multiple clinical trials
The Clinical Research Coordinator (CRC) responsibilities include:

  • execute and coordinate daily clinical research activities according to SOPs, GCP and FDA/ICH guidelines
  • ensures IRB approved protocols are implemented and followed
  • executes informed consent process and monitors patient status and safety
  • collects and organizes research data
  • educates patients about treatments and possible side effects

The Clinical Research Coordinator must also be able to perform or willing to learn clinical tasks -IV administration, injections, phlebotomy, EKGs, vital signs, etc.)

  • Obtaining informed consent
  • Patient screening and recruitment
  • Patient enrollment
  • Conducting study visits
  • Completing and ensuring the quality of case report forms, EDC
  • Maintaining source documents
  • Arranging necessary tests and procedures in accordance with protocol requirements

REQUIREMENTS:
LPN, MA, or RN
High degree of organizational skills.
Requires meticulous attention to detail.


Indeed - 11 months ago - save job - block
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