- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic...US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role… more
- Merck & Co. (Rahway, NJ)
- … Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology ... Clinical Research group and in the field...safety and efficacy as well as new drug applications, clinical study reports, or publicationsParticipation in internal… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …resolve or escalate to appropriate Governance Committee. Analyze CRO performance trends within a clinical study or across several studies and resolve or ... centered around rare diseases and immune disorders. Job Summary: Senior clinical operational leader accountable for operational...clin pharm patient studies , and Phases 1-3 clinical trials at the study and program… more
- Merck & Co. (Rahway, NJ)
- …(Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. ... support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal and joint… more
- Novo Nordisk Inc. (Boston, MA)
- …relevant to Rare Renal, and competitive products Understand the most recent approved clinical studies to educate customers as well as anticipate and (where ... areas. The STARS team collaborates and partners with groups across NAO, Research & Early Development, Development, innovation hubs across NN, other affiliates, and… more
- Merck & Co. (Rahway, NJ)
- …internal teams and external partners, design non-interventional and data synthesis studies , author study protocols, develop measurement questionnaires, case ... position resides within our company's Value and Implementation (V&I), Outcomes Research organization, which is responsible for real-world evidence generation and… more
- Merck & Co. (South San Francisco, CA)
- …through licensure. The role involves verifying data, writing pharmacology study reports, written summaries, and related documents, managing author/management ... Experience and Skills: Strong writing skills and experience drafting study reports, scientific manuscripts, or scientific documents Experience with laboratory… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with Novo Nordisk policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...claims data analysis Proven experience in leading and managing research partnerships. Experience running large-scale partnership studies … more
- Merck & Co. (Rahway, NJ)
- …'end-to-end' integrated clinical supply chain across the full of our company's Research Laboratories portfolio of clinical trial s .- GCS is accountable for ... - Responsible and accountable for establishing the timelines for clinical supply needs per study and providing...analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Works… more
- Merck & Co. (Rahway, NJ)
- …and publish articles in scientific journals.Track use of real-world evidence/outcomes research study results to inform decision-making.Maintain awareness of new ... research activities linked to V&I goals. Responsible for study -related contracting, budgets, and vendor/partner management.Support market affiliates to develop… more
