We are seeking a dedicated Clinical Research Coordinator to join our team. The individual will be responsible for managing and coordinating clinical trials and research studies in compliance with regulatory guidelines and protocols.
This role involves working closely with principal investigators, research staff, and study participants to ensure the smooth operation of the clinical research process.
Key Responsibilities :
- Coordinate and oversee all aspects of clinical trials, including participant recruitment, enrollment, and follow-up.
- Assist in the development of study protocols, consent forms, and data collection tools.
- Ensure all research activities comply with ethical standards, institutional policies, and regulatory requirements (FDA, GCP, IRB).
- Collect, manage, and analyze clinical data; maintain accurate and organized records.
- Communicate with study sponsors, monitor study progress, and resolve any issues that arise.
- Schedule and conduct participant visits, ensuring compliance with study protocols.
- Assist with the preparation of regulatory documents and reports.
- Maintain confidentiality and protect the integrity of participant data.
Clinical Research Coordinator 224410
We are seeking a dedicated Clinical Research Coordinator to join our team. This role involves working closely with principal investigators, research staff, and study participants to ensure the smooth operation of the clinical research process. The individual will be responsible for managing and coor...
Clinical Research Coordinator I - Medicine/Endocrinology
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I ...
Clinical Research Coordinator
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
Clinical Research Coordinator
This is a clinical research position partially funded by a Shriners Hospitals Clinical Outcomes Studies research grant. Position responsibilities include: provide support and ensure site compliance with the Grant Proposal; assemble / process / coordinate approval for The Home Office and local Human ...
Clinical Research Nurse Coordinator II, Oncology
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
Clinical Research Coordinator Assistant
The assistant clinical research coordinator (CRC) is responsible for assisting more senior staff with several aspects of the conduct of clinical trials, including (but not limited to): subject recruitment, screening, enrollment, scheduling, physical performance testing, data collection, participant ...
Clinical Research Coordinator II - Pediatric Neonatology - Full-Time, Hybrid
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on e...
Clinical Research Coordinator II (Oncology)
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
Clinical Research Coordinator I - Kerlan Jobe Institute
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Clinical Research Coordinator I - Obstetrics & Gynecology - Maternal-Fetal Medicine (Part-Time, Hybrid)
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...