What are the responsibilities and job description for the Clinical Research Coordinator position at IntraCare?
About IntraCare
IntraCare Health Center (DFW Healthcare MSO) proudly serves the greater Dallas-Ft. Worth and Phoenix, Arizona areas with a decade of excellence in value-based care and clinic operations. Our outstanding leadership and commitment to service have established us as a trusted partner for multiple healthcare organizations.
At IntraCare, we believe in more than just a job; we offer a vibrant workplace where culture and collaboration thrive. We are dedicated to fostering an inclusive environment that values diverse perspectives and promotes respectful dialogue. Our approach encourages innovation and healthy debate, as we seek to build a team of dedicated partners who contribute to our collective success. We are passionate about empowering our employees, helping them grow both personally and professionally. This unwavering focus on team culture and individual development is the cornerstone of our ongoing achievements.
About the role
About the Role : We are looking for a meticulous and proactive Clinical Research Study Coordinator to join our dynamic team. In this role, you will oversee and coordinate various aspects of clinical trials, ensuring adherence to regulatory standards and study protocols. You will collaborate closely with the research team, and participants to facilitate the successful execution of research studies.
What you"ll do
Key Responsibilities :
- Oversee all phases of clinical trials, including participant recruitment, informed consent processes, and data collection.
- Maintain comprehensive and organized study documentation, such as case report forms, regulatory paperwork, and study logs.
- Schedule and conduct study visits, follow-ups, and assessments with participants.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and study protocols.
- Communicate effectively with Principal Investigators, research staff, and study sponsors to ensure smooth operations.
- Monitor the progress of studies and report any issues or deviations to the Principal Investigator and sponsor.
- Assist in the preparation of study-related documentation, including protocols, informed consent forms, and regulatory submissions.
- Perform data entry tasks while ensuring data integrity and confidentiality.
- Organize and participate in study meetings, training sessions, and site visits.
Qualifications
If you are detail-oriented and passionate about clinical research, we invite you to apply and contribute to our mission of advancing medical knowledge through rigorous and ethical research.
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