- Bristol Myers Squibb (Princeton, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Manager , Clinical Data Management (Data Management Lead) is ... Director, Clinical Data Management or Associate Director, Clinical Data Management (Line Manager ) within the...is responsible for: **Project Management and Leadership** + Provides clinical data management leadership within the study … more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Senior Manager , Clinical Data Management, Bristol-Myers Squibb Company, ... Princeton, NJ.** Provide clinical data management leadership within the study team to align and drive data collection requirements for complex clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …partnership with GDO protocol manager ; and collaborate with cross functional study team members + May support clinical development planning (collaboration ... narratives + Provision of information required by Protocol Manager for development of trial budget, CRO scope of...committee (eg, DMC) activities + Drafting/review and validation of clinical study reports (CSRs) and clinical… more
- Merck (West Point, PA)
- …the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and ... operational plans for all activities associated with clinical supplies for their assigned studies , which...+ Responsible and accountable for establishing the timelines for clinical supply needs per study and providing… more
- J&J Family of Companies (Spring House, PA)
- …Medicine (TM) and Translational Science (TS). TM has combined expertise in the clinical study of immunologic disease, immunologic pathways, and in early ... study results. In this position the Executive Director/ Senior Director will be accountable for providing an environment...Direct and supervise the preparation and review of protocols, clinical study reports, clinical pharmacology… more
- Merck (West Point, PA)
- …Management Section of the GCS Planning organization. Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... strategic and operational plans associated with the downstream activities of clinical supplies for their assigned studies . The primary function of the IM CSPM is… more
- Novo Nordisk (Plainsboro, NJ)
- …activities align with the highest standards of scientific rigor and ethics. The Senior Global Medical Manager will drive and collaborate with cross-functional ... and support health care professionals though robust medical education initiatives. The Senior Global Medical Manager will leverage data-driven insights and… more
- Merck (West Point, PA)
- …operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have ... development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Senior Manager , Statistical Programming, Bristol-Myers Squibb Company, Princeton, ... submission deliverables in compliance with published industry standards and project/ study -specific requirements. Review key planning documents (eg, statistical analysis… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Senior Manager , Tax Operations (Federal) **Location** : Lawrenceville, ... New Jersey **Position Summary** As a Senior Manager , Tax Operations, you will be...consultants, organizing and gathering source information, managing tax return studies and tax software administration. Provide support for the… more
- J&J Family of Companies (Horsham, PA)
- …marketing commitments in assigned therapeutic areas. This individual will be the line manager for the Clinical Operations and Program Management (PM) team and ... more at https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical Trial Project Management **Job Category:** People Leader **All Job… more
- Novo Nordisk (Plainsboro, NJ)
- …aligned therapeutic / franchise area(s). Relationships Reports to the Director/ Senior Director of Value Communication and Contracting Strategy. Interacts frequently ... in collaboration with internal management and senior level global stakeholders. Interacts internally with Strategic Pricing & Contracting, Finance, Brands, Medical… more
- J&J Family of Companies (Spring House, PA)
- …and finalize clinical documents such as, but not limited to, clinical study reports, investigator's brochures, study protocols, summary documents, ... industry, company, and regulatory guidelines. **Principal Relationships:** + Internal: manager , other writers cross-functional contacts (eg, clinical ,… more
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Global Medical Affairs Senior Director, Gastroenterology **Location:** Cambridge, MA **Level** : L4-2 **Hiring Manager :** Cristina Almansa **About ... be responsible for medical affairs activities for phase IV studies and Life Cycle management activities. With guidance from...indication; define and prioritize the future needs including new study ideas and tactics to prioritize the best areas… more
- BeiGene (Trenton, NJ)
- …data protection. The Sr. Document Specialist will assist in closure and archival of clinical studies , as necessary, and management of the storage systems and ... Description:** The Sr. Document Specialist, Global Records works with Global Records Manager to operationalize Records Management within Global R&D and the Trial… more
- Novo Nordisk (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... difference? The Position The HEOR Strategy and Evidence Synthesis Manager will be part of the HEOR Evidence Synthesis...and. The HEOR-ESS sub-team is part of a larger Clinical Data Science and Evidence (CDSE) team which sits… more
- RELX INC (Horsham, PA)
- …better humankind. For more information, please visit www.reedtech.com About the role The Senior Manager , GxP Quality Systems, is responsible for overseeing and ... to ensure compliance with Good Practice (GxP) regulations, including Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Good Laboratory Practice… more
- Sanofi Group (Bridgewater, NJ)
- …of efficacy, immunogenicity and safety data. Lead the interpretation and critical evaluation of study results. Review clinical study reports and clinical ... for regulatory submissions. + For CTD preparation following Global Medical-led registration studies : + Responsible for the review of clinical sections of… more
- Novo Nordisk (Plainsboro, NJ)
- … clinical activities beyond phase 3a (phase 3b workshops, Investigator Spon- sored Studies ) + Evaluation and decision of clinical trial proposals from Regions ... MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D… more
- RELX INC (Trenton, NJ)
- …with a diverse range of internal and external stakeholders, including senior -level executives. + Showcase proficiency in strategic account planning and management, ... prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate… more