Clinical Research Coordinator

Job Summary

The Clinical Research Coordinator (CRC) is responsible for coordinating ongoing clinical research projects within the South Shore Health Center for Wound Healing. The CRC will be responsible for identifying and recruiting patients eligible for participating in the trials, obtaining informed consent, collecting and entering data, maintaining patient study files in accordance with legal and institutional guidelines, entering data into sponsor-specific electronic data capture forms, reconciling wound research billing, and, performing administrative tasks. The CRC will serve as the primary contact with patients enrolled in clinical trials at the center, will liaise with trial sponsors, support studies from start up to closure, and will be responsible for complying with Institutional Review Board (IRB) requirements. The CRC will also support internal and external monitoring needs and quality improvement projects. The CRC will report to the Principal Investigator of several wound research studies and will be expected to support project needs to ensure trials stay on track.

 



Qualifications

Candidates with a Bachelor’s degree in a scientific, health related, or business administration program, preferred. At minimum, a candidate must have a Bachelor’s degree.  Minimum 2-3 years in a clinical research environment preferred. 

 

(Employees new to a position have 6 months to attain these required classes/skills)

 

  • Must be proficient in Microsoft Office Word and Excel, electronic health systems and databases used in research environment, or have a willingness to learn and demonstrate proficiency within six months of hire

  • Must be proficient in filing submissions with the IRB within six months of hire

  • Must be proficient in research billing and reconciliation in EPIC.


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