- Daiichi Sankyo, Inc. (Bernards, NJ)
- …coordinated and aligned strategy.Responsibilities:Operational Strategy and Oversight:Align with the Senior Director , Global Clinical Operations on plans for ... SOPs. The Director will ensure the Senior Director , Clinical Operations (Asset Lead) is fully...to their program . May on occasion represent Global Clinical Operations on the Strategy and… more
- Insmed Incorporated (NJ)
- …labeling, distribution, returns, reconciliation, destruction, and logistics for global clinical programsDefine and implement comprehensive sourcing ... future of science, we're in. Are you?About the Role:The Director of Clinical Supply Chain Operations is...Clinical Supply Chain Operations is responsible for leading global demand planning and ensuring the successful delivery of… more
- Insmed Incorporated (NJ)
- …a professional manner to executive audiences including attendance at requested meetings (ie, Global Clinical Team, Global Project Team, etc.)Who You ... Represents Clinical Operations in a range of cross-functional groups, global functional committee(s) and initiatives intended to enhance function and company… more
- Insmed Incorporated (NJ)
- …other, and for the future of science, we're in. Are you?About the Role:The Director , Global Medical Training Strategy will be responsible for developing the ... role will ensure the training needs for assigned products are met across all of Global Medical Affairs. The Director , Global Medical Training Strategy will… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our company ... development teams and the operational/executional arms within the business.- - The Program Clinical Supplies Project Manager ( Program CSPM) serves as the… more
- Insmed Incorporated (NJ)
- …upon evaluation of credentials and experience . Lead development and execution of global regulatory strategies for clinical , pre- clinical , and lifecycle ... global CTA submission strategiesDirect the planning and coordination of global regulatory submissions, including clinical trial applications for multinational… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Compliance will be responsible for providing quality oversight over the compliance program within the global quality organization to ensure harmonization, ... across all functions and sites.Support the development of the GMP Compliance program related to clinical / commercial stage and manufacturing.Support Legend's… more
- Novo Nordisk Inc. (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 ... The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their...and VP with other operational units across NNI and global functions; Drive effective decision-making within CDSE senior leadership… more
- Eisai, Inc (Nutley, NJ)
- …and monitor study data.Implements strategies to identify, monitor and resolve clinical program /trial issues.Interprets study data and develops integrated ... If this is your profile, we want to hear from you. The Director , Clinical Pharmacology actively contributes to multi-disciplinary teams by providing innovative… more
- Eisai, Inc (Nutley, NJ)
- …(QAP) position is responsible for design, delivery and execution of the global Clinical Quality Assurance (CQA) strategy including audit and inspection ... potential. Essential Functions Direct and drive design, delivery, and execution of the global Clinical Quality Assurance (CQA) strategy for the country/region in… more
- Insmed Incorporated (NJ)
- …patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare ... we're in. Are you?About the Role:This is a REMOTE position. The Associate Director of Field Medical Excellence (FME) will implement field medical functional strategy… more
- Insmed Incorporated (NJ)
- …You'll Do: Participate in cross functional teams to develop and implement Clinical Study protocols within clinical program (s). Responsibilities include ... so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of...of science, we're in. Are you?About the Role:The Associate Director , Clinical Research Scientist will support and… more
- Insmed Incorporated (NJ)
- …Sets tasks, prioritization, and resources within assigned compound(s) Provides program -level programming leadership and support to clinical development ... patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare… more
- Novo Nordisk Inc. (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 ... you ready to make a difference? The Position The Director , Real World Science leads the evidence strategy and...evidence planning, execution and synthesis with NNI stakeholders across Clinical Data Science & Evidence as well as within… more
- Insmed Incorporated (NJ)
- …patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare ... operations, enterprise risk management, and Computer Systems Validation (CSV) program . This role will manage cross-functional teams and ensure compliance… more
- Novo Nordisk Inc. (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 ... you ready to make a difference? The Position The Director Medical Review oversees a team of Medical Reviewers...within Patient Safety organization, CMR, outside of CMR, and Global Patient Safety and Safety Surveillance teams. Works closely… more
- Novo Nordisk Inc. (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 ... scalability, automation, and continuous improvement. Relationships Reports to the Executive Director , PS & GxP Business Operations. Accountable for establishing and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. SummaryThe Director Global Medical Affairs Oncology (GMA), ADC, under the direction ... of the Senior Director , GMA Oncology ADC ( Global Medical Affairs...More Years experience in pharma at local, regional and/or Global level. preferred- Excellent knowledge of current clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …work together to change lives for the better. The Position The Associate Director , Media Relations & Issues Management is accountable for establishing and leading ... potential to dramatically influence stakeholder perceptions. Relationships Reports to the Director , Media & Stakeholder Relations, and interacts with senior leaders… more
