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Clinical Research Coordinator Ii-Msh-Cs03-12118-013
Company | Mount Sinai Health System |
Address | United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-08-04 |
Posted at | 10 months ago |
Description
- Prepares and ensures grant applications, IRB/GCO documents are submitted.
- Performs other related duties.
- Mentors Clinical Research Coordinators in training.
- Independently obtains informed consent for other clinical studies.
- Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
- Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
- Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
- Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests.
- Ensures accurate and complete compilation of subject data through chart reviews.
- 2 years of clinical research
- Bachelors degree in sciences or related field.
- Serving as a role model confronting racist, sexist, or other inappropriate actions by speaking up, challenging exclusionary organizational practices, and standing side-by-side in support of colleagues who experience discrimination.
- Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
- Using a lens of equity in all aspects of patient care delivery, education, and research to promote policies and practices to allow opportunities for all to thrive and reach their potential.
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