- Bristol Myers Squibb (Madison, NJ)
- …leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... Director of Informed Consent Management. The AD will be responsible for informed consent activities and will also serve as the Global Process Lead for… more
- Novo Nordisk (Plainsboro, NJ)
- …profile + Develop and update the minimum mandatory safety text (MMST) for use in the Informed Consent + Own the safety sections of the labelling for the evolving ... Committees (ECs) regarding safety aspects of protocols and Patient Information (PI)/ Informed Consent (ICs) + Establish and ensure deliverables to/from Data… more
- The Mount Sinai Health System (Elmhurst, NY)
- …pursuant to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients for procedures, recalling patients for ... required professionally or at the request of the supervising physician(s), Director of Service, and/or Supervising Physician Assistant. *-indicates duty is… more
- The Mount Sinai Health System (New York, NY)
- …Myeloma (MM) Program at Mount Sinai hospital. In collaboration with the MM Medical Director , the Associate Director , and the clinical trials investigators; ... the research program. The Clinical Program Manager will report into Associate Director . **RESPONSIBILITIES** Administrative Responsibilities: + Works with… more
- The Mount Sinai Health System (New York, NY)
- …the Clinical Trials Office administration, the Clinical Research Coordinator will report to the Associate Director of the CTO and will be responsible for the ... below. **RESPONSIBILITIES** + Educating patients regarding study requirements and obtaining informed consent from research participants + Collection of study… more