Clinical Research Coordinator (Medical Devices)

Location: Orlando, Florida, United States
Salary: competitive
Job Type: Contract
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A Clinical Research Coordinator position is available at a Medical Device company with sites located Orlando, FL (via Real Staffing). This client's technology is focused on the treatment of chronic pain in a variety of applications including post-amputation pain, chronic post-surgical pain, and chronic migraine.

This is a long-term contract position that requires a commitment of 40hrs/week onsite in Orlando.

Responsibilities

  • Discuss study with patients and verify inform consent documentation
  • Provide patient with written communication of their participation (i.e. copy of signed informed consent)
  • Meet with patient for each visit and complete study source documentation worksheets for the PI
  • Enter data into an electronic database system
  • Adhere to GCP guidelines and study protocol requirements
  • Schedule patient for all study visits and procedures within guidelines/timeframes specified in the protocol
  • Complete and maintain the regulatory binder
  • Review CRFs against the patient's medical record for completeness and accuracy
  • Provide copies of hospital source document for serious adverse events, etc. to the Sponsor
  • Administer questionnaire and eDiary per protocol

Overall, this is a wonderful opportunity to join a growing organization during an exciting time. This person will join a fun team in a great environment, and will be able to work on innovative life-saving products.

If you are interested in learning more about this opportunity, apply to this advert and/or contact me on the details below!

Sthree US is acting as an Employment Business in relation to this vacancy.

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