- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …input into study protocol profiles, final protocols and amendments.Lead document review & coordination for the protocol and amendments. Additional medical writing ... bring deviations to the Operational program Lead and study team leader. Review and approve Vendor invoices, including investigator grants and pass through… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …input into study protocol profiles, final protocols and amendmentsLead document review and coordination for the protocol and amendments. Additional medical writing ... bring deviations to the Operational program Lead and study team leader. Review and approve Vendor invoices, including investigator grants and pass through… more
- SYSCO (Dubois, PA)
- …training sessions. Assist with the training of new employees as requested. Review and analyze daily and weekly reports such as special-order requests, customer ... bid files, and sales/gross profit margin data. Perform administrative duties, such as preparing sales budgets and reports, maintaining sales records, processing credits, and pick-up requests, preparing sales quotes and menu suggestions, and filing reports.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …strategic and planning alignment across regions and functions, and supports review of local country/regional Medical Affairs activities when applicable. Provides ... Operations and other cross-functional and regional stakeholders. Provides support in review of investigator-initiated studies (IIS) and may serve as deputy compound… more
- Aequor (Thousand Oaks, CA)
- …quality and related activities (eg, comparability, specifications, stability, annual product review ) in support of the Product Development Team (PDT). The PQL ... product quality of pivotal and/or commercial product(s) including timely product data review , ownership of GMP documents and regulatory filing sections, execution of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …privacy implications of business initiatives, product development, and marketing campaigns. Review relevant data protection agreements in coordination with Legal and ... observation and collection of facts. Conducts document collection, document and information review , interviews and/or other reviews of persons involved in or having… more
- Eisai, Inc (Nutley, NJ)
- …developing and executing the global medical affairs plan, including peer-reviewed review /perspective publications, medical education, support of symposia at major AD ... projects in the AD space with original contribution to drafting review /perspective articles for peer-reviewed journals; Liaise with external co-authors, internal… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …programs Serve as a leading member, or participant, at multiple internal review groups and utilize novel and creative methods to resolve clinical development ... and KOLs Interface together with VP Medical/Scientific Development with Safety Review Committees and Data Safety Monitoring Committees Participate in safety … more
- Merck & Co. (Rahway, NJ)
- …and/or support batch processing readiness and execution activities. Prepare, review , and/or approve GMP Documentation as appropriate. Author/Approve Standard ... share and align on best practices. Author lessons learnt through after action review summaries or other reports to capture knowledge gained. Drive new technology… more
- Eisai, Inc (Exton, PA)
- …early to late stage manufacturing programs.This position will be responsible for the review and interpretation of analytical testing data as well as protocols and ... company's discretion. Essential Functions Managing external testing lab collaborations 15% Review and interpretation of analytical data 20%Troubleshooting of analytical… more
