- Daiichi Sankyo, Inc. (Bernards, NJ)
- …product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors or oversees the ... development of the Safety Management Plan for assigned product(s)Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation. May contribute to safety action recommendations, and communication… more
- 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
- Pfizer (Pearl River, NY)
- …+ Work closely with other medical monitors to ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and company ... country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team for… more
- Institute of Electrical and Electronics Engineers (Piscataway, NJ)
- Associate Director , Digital Governance and Solutions - 240282 : MGT-B70 Description Job Summary The overall purpose of this position is to manage and enhance ... and templates for webmasters and marketing staff and volunteers. Collaborates with Director , Experience Design and business and IT stakeholders to contribute to… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s) + Authors or ... oversees the development of the Safety Management Plan for assigned product(s) + Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation. May contribute to safety action recommendations,… more
- Pfizer (Pearl River, NY)
- …fit with the clinical program strategy. + Ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and company ... Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare professionals at sites… more
- Pfizer (Pearl River, NY)
- …clinical program strategy. + Provides oversight to ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and ... + Supports Program specific training to study team, investigators, clinical research associate , and others. + Oversees interactions of clinical team with healthcare… 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 (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
