Clinical Research Coordinator Anesthesiology

Yale University-posted 2 months ago
$65,000 - $101,000/Yr
Full-time • Entry Level
New Haven, CT
5,001-10,000 employees
Educational Services
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Within the Department of Anesthesia, the Clinical Research Coordinator (CRC) will lead efforts in the execution of research studies within the scope of the established study protocol(s) assigned. These activities include, but are not limited to, study start up, patient screening, eligibility determination, registration, and other protocol and subject milestones. The CRC will also be the primary point of contact for the sponsor on all communications and management of all study and regulatory documentation. The CRC will have direct patient contact and will be responsible for managing multiple clinical research projects/trials and will serve as a back up to other clinical research coordinators within the clinical research team in Anesthesia. The CRC will work collaboratively with postgraduate and medical students. Some studies may require support on weekends/after normal business hours. Subjects will be recruited in New Haven and surrounding clinics/locations (currently Milford and New Haven), so some travel is required. The fixed duration time, does have opportunity to be extended upon completion.

  • Assumes primary responsibility for a program, service, activity, operation or function in an assigned area.
  • Coordinates day-to-day operations in order to achieve designated goals.
  • Ensures effective management and leads the development and implementation of best practices.
  • Designs and implements quality control metrics to identify areas of risk.
  • Analyzes, recommends, and implements strategic solutions to minimize risk.
  • Develops a variety of complex report and other written materials.
  • Provides guidance to and collaboration with internal and external partners as necessary.
  • Develops, oversees and monitors budgets.
  • Develops and maintains specialized training.
  • May perform other duties as assigned.
  • Demonstrated experience with informed consent.
  • Demonstrated experience coordinating execution of clinical trials.
  • Demonstrated knowledge of Good Clinical Practice (GCP) guidelines, applicable federal regulations, and institutional practices, standards, policies, and procedures at the unit/functional level.
  • Advanced interpersonal, oral, and written communications skills and ability to work effectively with a wide variety of external and internal stakeholders and on a team.
  • Strong computer skills required, including strong competency in Microsoft Office programs (Word, Excel, etc.) & excellent time management skills and organization.
  • Minimum requirement of Bachelor's Degree in related field and two years of related experience or an equivalent combination of education and experience.
  • Strong Knowledge of clinical and research data systems.
  • Proven experience in RedCap, OnCore, EPIC, and eReg are preferred.
  • Comfortable with basic handling of specimens including centrifugation, pipetting, labeling, and freezing.
  • Salary Range: $65,000.00 - $101,000.00
  • Full time position
  • Fixed duration with opportunity to be extended
  • On-site work model
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