- Merck & Co. (Rahway, NJ)
- …with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong negotiation, influencing, ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...the GCS Planning organization to customers both internal and external to GCS and serves as the lead GCS… more
- Merck & Co. (Rahway, NJ)
- …we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance ... medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle… more
- Merck & Co. (Rahway, NJ)
- …compounds.Support of business development assessments of external opportunitiesThe Senior Director May: Supervise the execution of clinical studies. Work ... to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …maintain collaborative relationships with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory ... and marketed products; required4 or More Years Knowledge of Good Clinical Procedures (GCP) and Good Pharmacovigilance Procedures (GVP) required4 or More… 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 ... to make a difference? The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their role, they will lead operations… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction ... of the Senior Director / Director , GMA Oncology (Global Medical Affairs team...medical information and internal education, publications, scientific exchange and external data communication, and stakeholder scientific engagement. Responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... instruct teams on how to properly conduct high quality clinical evaluation of signals in the appropriate tool (eg,...subject matter expert in cross-functional teams or committees and external environments at a global and regional level as… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …as we work together to change lives for the better. The Position The Associate Director , Media Relations & Issues Management is accountable for establishing and ... local and national levels, to position the company favorably among its key external audiences; and to ensure public understanding of the company's mission, business… 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 ... role of GxP Patient Safety, Compliance & Vendor Oversight within our Clinical , Medical & Regulatory (CMR) organization. This position combines the critical functions… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …ensure compliance with SDEA requirements. Relationships This position reports to the Associate Director , Safety Contracts & Supplier Management. This position ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...in Global Patient Safety and Contract Owners in NNAS. External relationships include interactions with NNI business partners, suppliers,… more
- Organon & Co. (Jersey City, NJ)
- …to meet project timelines. + Serving as the subject matter expert in the non- clinical field in meetings with internal/ external stakeholders + Author and review ... **Job Description** **The** **Position** The Non- Clinical Safety Assessment Representative within the Non- Clinical Development (NCD) team, is accountable for the… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance ... for the general medicines portfolio of products marketed worldwide. The Associate Director , Biopharmaceutics will also be responsible for contributing… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The role of Associate Director , Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters ... Director of Medical Affairs Outcomes Research. Focusing on Dermatology,...provide expertise in ensuring economic models communicated to all external stake holders including Health Technology Assessment (HTA) bodies… more
- Regeneron Pharmaceuticals (Warren, NJ)
- The Associate Director , External Data...+ A minimum of **10+ years of experience** in External Clinical Data Management, with expert knowledge ... and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data...structure. **A typical day in the life as an Associate Director , External Data Services… more
- System One (Basking Ridge, NJ)
- Job Title : Associate Director , Clinical Safety Scientist (Contingent Worker) Job Schedule: Candidate can work 100% remote - preference would be EST/CST ... perform safety surveillance and risk management for assets in early/late stage clinical development, as well as post-marketing, in partnership with Product Safety… more
- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful...(SMT), supporting trial leaders and interfacing with internal and external stakeholders to ensure compliance, quality, and timely delivery… more
- Bristol Myers Squibb (Princeton, NJ)
- …biology, mechanism of action, and predictive biomarkers in our late-stage clinical oncology portfolio. Ideal candidates will possess a strong scientific background, ... matrixed industrial environment. Seeking candidates with Biomarker Lead late stage clinical trials for Phases II/III preferred. Regulatory submissions drug approvals… more
- Merck (Rahway, NJ)
- …with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong negotiation, influencing, ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...the GCS Planning organization to customers both internal and external to GCS and serves as the lead GCS… more
- Bristol Myers Squibb (Princeton, NJ)
- …of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and ... immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial/biomarkers and asset development as well as disease research… more
