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
outcomes of the network. Our goal is to provide high quality, compassionate clinical care for every patient, every time.
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Job Title:
Clinical Research Coordinator
Requisition Number:
42785
Employment Type:
Full Time
Division:
EDUCATION & LIBRARY
Compensation Type:
Salaried
Job Category:
Nursing / LVN
Hours Worked:
8am-5pm
Location:
John Peter Smith Hospital
Shift Worked:
Day
Job Description:
Description: The Clinical Research Coordinator is responsible for assisting investigators with the conduct of new or ongoing intervention studies supported by the JPS Health Network Research Institute. This position is involved in intervention studies pertaining to injuries, chronic diseases, and infectious diseases.
Typical Duties:
- Assists with the development of research protocols, recruitment strategies, budgets, and data collection forms in collaboration with research team.
- Prepares regulatory reports and Institutional Review Board submissions and ensures compliance and preparedness for internal and external audits and study monitoring visits.
- Coordinates and manages intervention studies, including but not limited to participant recruitment and enrollment, data collection, development and use of case report forms, adverse events reporting, filing and archiving of study records, resolution of data queries, and communication with sponsors and regulatory authorities.
- Ensures participant safety and confidentiality throughout all phases of research.
- Trains staff and volunteers on the implementation of research protocols.
- Maintains databases and ensures timely and accurate documentation of study-related information.
- Assists with writing internal reports, as necessary.
- Rotates on a weekly on-call schedule to meet study needs.
- Attends investigator meetings that may require out-of-state travel, as needed.
- Performs other related duties as assigned.
Qualifications:
- Required Education and Experience:
- Bachelor's degree in a health-related field from an accredited college or university.
- 2 plus years of clinical research experience or 4 plus years of clinical nursing experience.
- Completion of human subjects protection training within 30 days of hire.
- If applicable, individuals with a professional license (e.g. nurses) must maintain current licensure.
- Master's degree in a health-related field from an accredited college or university.
- 2 plus years of experience in regulatory compliance and conduct of clinical trials.
- Certified Clinical Research Professional through the Association of Clinical Research Professionals or the Society of Clinical Research Associates.
Required Licensure/Certification/Specialized Training:
Preferred Education and Experience:
Preferred Licensure/Certification/Specialized Training:
Location Address:
1500 S. Main Street
Fort Worth, Texas, 76104
United States