- Genmab (Plainsboro, NJ)
- …with the teamReview and approve protocol and amendment changesReview the Master Informed Consent Form (ICF)Approve operational plans, manuals, and charters for ... the trialOversee the vendor selection processInitiate and verify the accuracy and completeness of initial Work Orders (WO) and Change Orders (CO)Guide the country selection processCoordinate responses to IEC/IRB commentsMonitor major protocol deviations (PDs)… 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
- 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
- Mount Sinai Health System (Jamaica, NY)
- …to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients, recalling patients for further evaluation ... required professionally or at the request of the supervising Attending Physician, the Director of Service, and/or Chief Physician Assistant. -The PA may perform the… more
- 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; ... of the research program. The Clinical Program Manager will report into Associate Director . **Qualifications** Education: + Bachelor's Degree (BSN) (required) or… more
- Weill Cornell Medical College (New York, NY)
- …this role when Hired for NYC Offices **Position Summary** Reporting to the Associate Director of the Office of Sponsored Research Administration, the Subawards ... of IRB and IACUC applications to ensure alignment with informed consent forms and contractual agreements. +...+ Provide ad hoc reports requested by the Executive Director of Research Business Operations, and perform other duties… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …remote position **RESPONSIBILITIES:** + In partnership with Clinical Program Manager or Associate Director , provides guidance and daily oversight for the ... and/or contributes to development of study-related documents (eg, Clinical protocols, Informed consent forms, Pharmacy Manual, Monitoring Plan, Case Report… more
