Clinical Research Coordinator
3 weeks ago
We are seeking a highly skilled Clinical Research Coordinator to join our team at the University of California, San Francisco (UCSF). The successful candidate will be responsible for coordinating clinical research studies, including study design, protocol development, and regulatory compliance.
Key Responsibilities
- Contribute to study design from a methodological standpoint
- Participate in the review and writing of protocols and study documents
- Ensure compliance with all relevant regulatory agencies
- Coordinate meetings with the study team
- Report study progress to investigators and other stakeholders
- Maintain finances and generate subcontracts
Requirements
- BA/BS with a major in a related field (e.g. biostatistics, public health, epidemiology)
- Graduate degree in epidemiology, biostatistics, statistics, nutrition, or public/global health
- Independence, planning, and decision-making abilities
- Proficiency with computers and software (e.g. Word, Access, Excel)
- Experience in clinical research or a related field
Preferred Qualifications
- Knowledge of NIH grant submission and management process
- Knowledge of relevant Federal and State regulations and policies
- Experience in writing, editing, and reviewing scientific manuscripts
- Proficient in French
About UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care.
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