Clinical Research Coordinator
Who We AreJPS Health Network is a $950 million, tax-supported healthcare system in North Texas. Licensed for 582 beds, the network features over 25 locations across Tarrant County, with John Peter Smith Hospital a Level I Trauma Center, Tarrant County's only psychiatric emergency center, and the largest hospital-based family medical residency program in the nation. The health network employs more than 7,200 people.
Acclaim Multispecialty Group is the medical practice group featuring over 300 providers serving JPS Health Network. Specialties range from primary care to general surgery and trauma. The Acclaim Multispecialty Group formed around a common set of incentives and expectations supporting the operational, financial, and clinical performance
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Job Title:
Clinical Research Coordinator
Requisition Number:
44013
Employment Type:
Full Time
Division:
EDUCATION & LIBRARY
Compensation Type:
Salaried
Job Category:
Nursing / LVN
Hours Worked:
Location:
Oncology & Infusion Center
Shift Worked:
Job Description:
Job Summary: The Clinical Research Coordinator is responsible for the independent coordination and management of complex clinical trials across multiple therapeutic areas. This role provides advanced clinical and operational support to Principal Investigators and serves as a key liaison between sponsors, regulatory bodies, and institutional departments to ensure the successful execution of clinical research studies. This position supports interventional trials sponsored by pharmaceutical, biotechnology, and medical device industries, and requires a high level of clinical judgement, regulatory knowledge, and organizational expertise.
Essential Job Functions & Accountabilities:
- Independently manages all phases of clinical trials, including start-up, activation, enrollment, maintenance, and close-out.
- Performs and oversees patient screening, recruitment, informed consent, and enrollment processes.
- Coordinates and conducts study visits in accordance with protocol requirements, including clinical assessments and specimen collection.
- Ensures compliance Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements (e.g. FDA).
- Serves as the primary point of contact for sponsors, monitors, and auditors, lead and support monitoring visits, audits and inspections.
- Maintains accurate and timely documentation, including source documents, case report forms, and regulatory documents, performing quality checks to maintain compliance.
- Identifies and proactively resolves protocol or operational issues, including recruitment barriers and protocol deviations.
- Monitors and documents adverse events and protocol deviations, reporting them to the Principal Investigator in a timely manner.
- Coordinates the scheduling of participant visits in accordance with the research protocol.
- Assists in the development of study-specific source documents and other materials required for proper implementation of the clinical trial.
- Provides mentorship and guidance to Research Associates.
- Collaborates with investigates and leadership to assess study feasibility and support study selection.
- Assists in budget development, and contract review, and resource planning as needed.
- Rotates on an on-call schedule to meet study needs.
- Attends investigator meetings that may require out-of-state weekday and/or weekend travel, as needed.
- Job description is not an all-inclusive list of duties and may be subject to change with or without notice. Staff are expected to perform other duties as assigned.
Qualifications:
Required Qualifications:
- One of the following qualification groupings is required for this position as indicated below:
- Master's degree in Public Health, Health Administration, Exercise Physiology or related field of study from an accredited college or University.
- 2 plus years clinical research experience.
- Completion of Human Subjects Protection, Good Clinical Practice, and IATA Training within 30 days of hire.
- Bachelor's degree in Public Health, Health Administration, Exercise Physiology or related field of study from an accredited college or University.
- 4 plus years of clinical research experience or current certification (CCRC, CCRP).
- Completion of Human Subjects Protection, Good Clinical Practice, and IATA Training within 30 days of hire.
- Bachelor's in Nursing from an accredited college or University.
- Current licensure by the Board of Nurse Examiners for the State of Texas or proof of reciprocity of licensure between the State of Texas and another state to be transferred to Texas within 90 days of employment.
- 2 plus years nursing experience in a healthcare setting.
- Completion of Human Subjects Protection, Good Clinical Practice, and IATA Training within 30 days of hire.
- OR
- OR
Preferred Qualifications:
- Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or equivalent.
- Experience in a multi-therapeutic clinical/clinical research environment.
- Bilingual: Spanish & English.
Location Address:
1450 8th Avenue
Fort Worth, Texas, 76104
United States