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Clinical Research Coordinator

Community Health Network

Indianapolis, IN

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JOB DETAILS
SKILLS
Administrative Skills, Behavioral Health, Business Support, Cancer, Candidate Screening, Case Report Form (CRF), Certified Clinical Research Coordinator (CCRC), Clinical Practices/Protocols, Clinical Research, Clinical Support, Community Health, Data Collection, Data Management, Electrocardiogram, Executive Assistant Skills , Financial Projections, GCP (Good Clinical Practices), Healthcare, Healthcare Providers, Hospital, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Interpersonal Skills, Laboratory, Laboratory Testing, Leadership, Legal, Maintain Compliance, Nursing, Organizational Skills, Phlebotomy, Plan Meetings, Problem Solving Skills, Procedure Development, Research Protocols, Safety Compliance, Sample/Specimen Processing, Society of Clinical Research Associates (SoCRA), Specimens/Samples, Supply Chain, Team Lead/Manager, Time Management, Training/Teaching
LOCATION
Indianapolis, IN
POSTED
30+ days ago

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Clinical Research Coordinator

Job Ref

2602538

Apply Today!

Category

Administrative & General Support

Department

Clinical Research Oncology

Schedule

Full-time

Facility

Cancer Center South

1440 E County Line Rd

Indianapolis, IN 46227

United States

Shift

Day Job

Hours

80 hours per pay period

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)

Why Community?

At Community Health Network, we build teams that deliver exceptional care through empathy, communication and collaboration. We consider ALL an integral part of the exceptional patient experience. We PRIIDE ourselves on not having employees but Caregivers. Join our Community as we make a difference in your community.

Caring people apply here.

Apply Today!

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About the Company

C

Community Health Network

Community Health Network was created more than 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.

COMPANY SIZE
5,000 to 9,999 employees
INDUSTRY
Healthcare Services
WEBSITE
http://www.ecommunity.com/