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Research Program Director - Tisch Cancer Institute
Company | Mount Sinai Health System |
Address | United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-08-21 |
Posted at | 9 months ago |
Description
- Create and maintain accurate and reliable data in the OnCore Clinical Trials Management System
- Assist in development and standardization of Protocol Review Monitoring Standard Operating Practices across health system
- Create and maintain documentation of all PRMS activities and communications.
- Organize and manage bimonthly regular meeting using Zoom and electronic voting
- Serve as the main point of contact and subject matter expert for Protocol Review and Monitoring System (PRMS) of the Tisch Cancer Institute at Mount Sinai
- Facilitate the annual scientific progress, accrual monitoring, and amendment review of all cancer related studies
- Demonstrate expertise in understanding federal and regulatory guidelines as it applies to clinical research at the Tisch Cancer Institute
- Supply guidance to Protocol Review Committee members regarding the required levels of review, issues with protocol language and adherence to the myriad rules and regulations designed to protect research science integrity
- Work in conjunction with internal departments to ensure regulatory and statutory requirements are implemented in pre-PRMS processes within mandated timeframes
- Research, interpret and analyze cancer-related protocols and documents to ensure compliance with National Cancer Institute requirements for a NCI Designated Cancer Center
- Identify potential areas of improvement in the committee’s functions & progress and discuss corrective actions with cancer leadership
- Provide timely instruction to faculty investigators and research staff on the Protocol Review and Monitoring process
- Manage and guide the DFG Coordinator as needed in daily operations
- Experienced with virtual meeting formats
- Detail oriented
- Comfortable leading meetings
- Bachelors degree, Masters strongly preferred, in sciences or related degree
- 3 years supervisory
- Able to work independently
- Experience in clinical research, preferably in cancer.
- 7 years experience in a hospital/medical environment
- Strong written and verbal communication skills
- 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.
- 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.
- Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
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