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JOB DETAILS

Clinical Research Coordinator

CompanyCommunity Health Network
LocationIndianapolis
Work ModeOn Site
PostedNovember 7, 2026
About The Company
Community Health Network was created 60 years ago by our neighbors, for our neighbors. We've never forgotten that heritage. To this day, we're still locally based and locally controlled, and we're as closely tied to our communities as ever. As a non-profit health system with more than 200 sites of care and affiliates throughout Central Indiana, Community’s full continuum of care integrates hundreds of physicians, specialty and acute care hospitals, surgery centers, home care services, MedChecks, behavioral health and employer health services. At Community Health Network, we build teams that deliver exceptional care through empathy, communication, and collaboration. Caregivers play a vital role in our mission as they fulfill our PRIIDE values: Patients First. Relationships. Integrity. Inclusion. Diversity. Excellence. Exceptional Care - For Everyone We want to ensure that each patient, employee, physician, and volunteer feels welcomed, comfortable, and included in our environment at all times. We value different perspectives and welcome conversations about race, gender, religion, sexual orientation and culture. Because it takes everyone to build healthier communities. Our promise of Exceptional care. Simply delivered. means we strive to provide culturally-competent care that meets your individual needs.
About the Role

 

Join Community
Community Health Network has an excellent opportunity available within our clinical research department. If you are looking for challenging work and meaningful advancement, then you should consider a career with Community.

Make a Difference 
The Clinical Research Coordinator will be responsible for assessing, planning, implementing, and executing clinical research protocols in conjunction with the Principal Investigator and clinical research team

Your Exceptional Qualifications

  • Research Coordinator Duties: Identifies and screens appropriate candidates for eligibility for research studies. Obtains informed consent from eligible patients for a research study. Maintains an effective data management system to track study participants and activities. Collects data and completes case report forms and data queries as specified by the study protocol. Prepares source documents for data collection. Assists in identifying study related procedures for the project budget. 

    ·        Administrative Duties: Attends Investigator and Coordinator Meetings as requested by the sponsor along with appropriate department, division and/or service line meetings. Assists in determining facility, staff and supply needs required for set-up and implementation of a new study. Prepares for and is present for sponsor representative site visits. Serves as an educator and resource person for patients, family, staff and physicians.

    ·        Laboratory Duties: Performs phlebotomy, ECG and other testing, as needed after trained. Prepares and processes laboratory specimens for shipment according to study lab manual. Reviews labs and ancillary tests; and reports results to Principal Investigator and appropriate personnel in timely manner.

    ·        Interpersonal Skills: Effectively problem solves and informs Manager and Principal Investigator when appropriate.

    ·        Communication: Communicates on a regular basis with the Investigators, Research Team, Hospital Staff, Monitor and other sponsor representatives to ensure adherence to Good Clinical Practice (GCP) guidelines.

    ·        Safety & Compliance: Coordinates, implements and completes clinical research studies in accordance with protocol guidelines, GCP, ICH, local, state and federal standards. Monitors adherence to protocols, and reports violations in a timely manner to the sponsor and the IRB.

    ·         Individuals may not perform all of these duties, or may perform additional, related duties not listed here.

EDUCATION

  • 2 year / Associate Degree (Required)
  • 4 year / Bachelor's Degree (Preferred)
  • In lieu of the above education requirements, a combination of experience and education will be considered.

LICENSE & CERTIFICATION REQUIREMENTS

  • within three (3) years from hire Certifications/Licensures: (Certified Clinical Research Associate (CCRA - ACRP), Certified Clinical Research Coordinator (CCRC-ACRP), Certified Clinical Research Professional (CCRP-SoCRA))

EXPERIENCE

  • Previous experience in data abstraction is helpful (Preferred)
  • Minimum of 2 years in a related field of healthcare (Required)
     
Key Skills
Clinical researchData managementInformed consentPhlebotomyECGProtocol complianceGood clinical practiceData abstractionPatient educationSpecimen processingRegulatory complianceIRB reportingCase report formsBudget assistance
Categories
HealthcareScience & ResearchAdministrative
Job Information
📋Core Responsibilities
The Clinical Research Coordinator is responsible for executing clinical research protocols, including screening candidates, obtaining informed consent, and managing study data. They also perform laboratory duties such as phlebotomy and ECG while ensuring adherence to Good Clinical Practice and regulatory standards.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
8997
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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