Research Coordinator

Cone Health

High Point, NCFull-timePosted May 6, 2026

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Qualifications

  • •Required: Bachelor's degree OR Associate's Degree (with 2 yrs experience) OR Healthcare/Health-related certification, e.g., EMT, Pharm Tech, Rad Tech, etc. (with 4 yrs experience)
  • •Required: 4 Years (education and/or experience)

Responsibilities

  • •In close partnership with study volunteers and colleagues, the Clinical Research Coordinator plays a key role in managing the routine activities of clinical research, which involve the acquisition, organization, documentation, and assessment of research information
  • •Operating under supervision, this job involves supporting the researcher in coordinating follow-up meetings with subjects, executing clinical obligations, producing research paperwork, summaries, and diagrams, maintaining accurate records, overseeing participant tracking, and assembling study supplies
  • •Reviews patients for compatibility with study protocols, confirming that only qualified individuals are selected for participation in medical trials, ultimately improving the integrity and reliability of research findings
  • •Communicates with individuals involved in the study to elucidate the study's intent and acquires consent based on complete information, nurturing transparency and building confidence with patients and their families during the research journey
  • •Compiles data from a variety of outlets, such as patient records, medical files, interviews, and tests, to produce detailed documentation that ensures the precise and dependable evaluation of research information
  • •Maintains patient health records by completing documentation in the electronic health/medical record system when appropriate
  • •Manages several uncomplicated clinical trials at once, efficiently organizing and supervising different research activities to optimize the use of resources and ensure the timely implementation of research protocols
  • •Undertakes the role of a study coordinator overseeing pharmaceutical and/or device trials, skillfully organizing site initiation visits, monitoring visits, and close-out visits, and guaranteeing adherence to protocol standards and regulatory mandates
  • •This role supports the regulatory compliance of research projects by helping with the submission of study protocols, consent forms, and recruitment materials to the Institutional Review Board and department for approval
  • •Undertakes clinical duties, including tasks such as electrocardiography (ECG), pulmonary function testing (PFT), blood drawing (phlebotomy), administering medicines, etc., with supervision from the primary investigator, where allowed by state and licensing constraints
  • •Executes any other responsibilities as instructed
  • •8 more items(s)
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