Research Program Administrator - Heart Institute - Cheng Lab
About The Position
The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to an increasing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes. What will you be doing in this role? The Research Program Administrator works with the Principal Investigator or Department Head to coordinate all aspects of building a research program. This will included, development of infrastructure, overseeing clinical research staff, quality assurance, and coordination of grant activities and grant proposals. Administrator will identify improvement areas, prepare policies, train staff, and audit procedures to create an efficient clinical research program. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Requirements
- Works with the Principal Investigator or Department Head to coordinate all aspects of building a research program.
- Development of infrastructure.
- Overseeing clinical research staff.
- Quality assurance.
- Coordination of grant activities and grant proposals.
- Identify improvement areas.
- Prepare policies.
- Train staff.
- Audit procedures to create an efficient clinical research program.
- Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Responsibilities
- Coordinate all aspects of building a research program.
- Development of infrastructure.
- Overseeing clinical research staff.
- Quality assurance.
- Coordination of grant activities and grant proposals.
- Identify improvement areas.
- Prepare policies.
- Train staff.
- Audit procedures to create an efficient clinical research program.
- Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
