- Merck & Co. (Rahway, NJ)
- …and prepares , analy ze s , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Responsible and accountable ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...(GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our Company's Research Laboratories portfolio… more
- Merck & Co. (Rahway, NJ)
- …chain deliverables and prepares , analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders. Works directly in the ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...(GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full of our Research… 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 ... experience data (PED) evidence to support optimization of access & reimbursement, clinical practice, product development and registration. The Director serves as a… 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 PositionThe Novo Nordisk Real World Evidence (RWE) / Clinical Data Science & Evidence (CDSE) - Fellow is...and presentation. Demonstrate an ability to perform medical accuracy review with strong attention to detail. Proficiency in Microsoft… 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 ... development and implementation of strategies to maintain efficient and compliant Promotional Review Board (PRB) process Serve as a primary regulatory advertising and… more
- Merck & Co. (Rahway, NJ)
- …at governance for the Cardiovascular & Respiratory portfolio (discovery therapeutic area review , early and late-stage clinical governance), and fully supportive ... Area and strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic oversight for the early … more
- Merck & Co. (Rahway, NJ)
- …opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions, ... will preferably have experience with high concentration biologics to support clinical and commercial development. Maintaining a strong network internally and across… more
- Merck & Co. (Rahway, NJ)
- …potential medical breakthroughs.Support statistical programming activities for Early Oncology clinical development projects. Review the quality and reliability of ... statistical analysis and high-quality data to support decision making in clinical trials.Responsible for the development and execution of statistical analysis and… more
- Merck & Co. (Rahway, NJ)
- …to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate our ... have a medical contact within the company.Upon request from Global Clinical Trial Operations (GCTO), support Company-Sponsored Trials to enhance the understanding… more
- Merck & Co. (Rahway, NJ)
- …stakeholders across organizations such as Regulatory CMC, formulation functions, and clinical functions to ensure timebound progression of portfolio, initiatives for ... driving the development of in vitro-in vivo relationships and preclinical-to- clinical translation in bioperformance of formulationsThe Director will report to… more
- Merck & Co. (Rahway, NJ)
- …Development Team, Global Brand and V&I Outcomes Research leads to define clinical development plans and brand strategies for assigned TAsProvides a solid ... as relevant members to the Product Development sub-teams (Value Evidence, Clinical , Commercial, Publications and Label teams)Aligns medical plans and activities with… more
- Genmab (Plainsboro, NJ)
- …in the conduct of clinical trials in oncology. Proficiency in clinical data review and interpretation.Solid experience in translating medical/ clinical ... market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross functional teams.We have a… 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 ... development, effective execution of CMR foundational and role-specific/technical training (eg clinical trial-related, GxP, Compliance, etc.) across the US and Canada… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …associated mitigation plans to management and other internal stakeholders Perform regulatory review of all clinical and nonclinical documents for submissions, ... 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
- Merck & Co. (Rahway, NJ)
- …a Global Labeling Lead, you will guide cross-functional teams in the creation, review , and approval of Core and Local Labeling documents.You will be responsible for ... relevant pharmaceutical industry experience (eg, Medical Affairs, Regulatory Affairs, Clinical , Pharmacovigilance).Current Employees apply HERE Current Contingent Workers apply… 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 ... local and global publication stakeholders, including colleagues from Medical Affairs, Clinical Data Science & Evidence, legal, regulatory affairs, global publication… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Identify opportunities for improvement within the customer campaigns and engagement. Review and interpret campaign/tactic data to inform adjustments on customer ... Proven knowledge of the pharmaceutical industry, including medical, regulatory, clinical processes and market dynamics, especially within specified therapy area… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …pricing scenarios and strategy for all pipeline products starting in Phase II clinical trials Leads assessment of investments in payer contracts and patient copay ... issues impacting Novo Nordisk profitability of franchise area Leads the yearly review of current pricing strategies and owns the process for developing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …as well as the full range of treatment options available and associated clinical outcomes Leverages detailed knowledge of both Novo Nordisk and competitor products ... customer account approaches Follows-up with internal and external stakeholders to review product value, quality of care and account satisfaction Physical… more
- Tris Pharma (Monmouth Junction, NJ)
- …Legal team.The Contracts Manager/Paralegal supports the Legal department in the review , drafting and compilation of varied and complex business contracts across ... types and agreements (ie, NDAs, service agreements, supply, sales and clinical vendor agreements, etc.) Experience handling multiple aspects of legal support… more
