What are the responsibilities and job description for the Research Study Coordinator- FT Days position at White Rock Medical Center?
Job Description
Job Description
Description :
White Rock Medical Center is a community-based hospital located near the historic White Rock Lake community, that serves the Dallas, Garland, Mesquite and surrounding areas. We specialize in a wide range of services including comprehensive medical / surgical care, bariatric, cardiology, outpatient and emergency medicine.
Our mission is to deliver exceptional healthcare with compassion and excellence.
White Rock Medical Center is seeking compassionate, care-minded individuals to join our company and make a difference. As a member of the White Rock Medical Center team, you can advance your skills while working in a supportive and patient focused environment.
Apply today!
Why join White Rock Medical Center?
Competitive salary and benefits
Employee programs and events.
Paid Time Off and 7 Company Holidays.
Employer paid life insurance.
Additional voluntary benefits such as STD, LTD, etc.
Job Summary
The Research Study Coordinator is responsible for the coordination, administration, and execution of clinical research studies within a healthcare facility. Their role involves collaboration with research teams, healthcare professionals, sponsors, and study participants to ensure the successful implementation and conduct of research projects while adhering to regulatory and ethical standards. A Research Study Coordinator is a vital member of a healthcare research team, contributing to the advancement of medical knowledge and patient care by ensuring the successful conduct of clinical research studies.
Essential Functions
- Study Planning and Design :
- Collaborate with Principal Investigators (PIs) and study sponsors to develop research protocols and study plans.
- Assist in the creation of study budgets and timelines.
- Participant Recruitment and Informed Consent :
- Identify and recruit eligible study participants.
- Obtain informed consent from participants and provide information about the study.
- Maintain contact with study participants and manage their study-related activities.
- Data Collection and Management :
- Collect and record data as per the study protocol.
- Ensure the accuracy and integrity of study data.
- Maintain organized and confidential study records.
- Regulatory Compliance :
- Maintain awareness of regulatory requirements and ethical standards (e.g., FDA, ICH-GCP, HIPAA) and ensure compliance.
- Prepare and submit required regulatory documents for study approval and monitoring.
- Coordination and Communication :
- Coordinate study activities with other research staff and healthcare professionals.
- Act as a liaison between the research team, study sponsors, and relevant stakeholders.
- Provide regular updates and reports to PIs and sponsors.
- Study Monitoring and Quality Control :
- Implement quality control measures to ensure data accuracy.
- Monitor study progress and resolve issues as they arise.
- Participate in site visits and audits by regulatory authorities or sponsors.
- Adverse Event Reporting :
- Report any adverse events or deviations from the study protocol to the appropriate authorities and ethics committees.
- Documentation and Reporting :
- Maintain comprehensive study documentation and records.
- Prepare and submit study progress reports as required by regulatory agencies and sponsors.
Communication / Knowledge
Collaboration / Teamwork
Requirements : Experience
Education / Licensure and Certification
