- Merck & Co. (Rahway, NJ)
- …Inventory Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) ... per protocol and ensuring a robust signal for packaging and distribution for Clinical Finished Goods (CFGs)-Analyzes and anticipates project risks as they relate… more
- Merck & Co. (Rahway, NJ)
- …the operational/executional arms within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs ... non-our company marketed products . - Analyzes and anticipates project risk s as they relate to clinical...analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Works… more
- Merck & Co. (Rahway, NJ)
- …development teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the ... effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong… more
- Merck & Co. (Rahway, NJ)
- …presentation skills - Education/Experience Bachelor's Degree +5 years of pharmaceutical , clinical drug development, project management , and/or medical field ... . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data...OR Master ' s Degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical… more
- Merck & Co. (North Wales, PA)
- …Word, Outlook, etc.)Education/Experience: Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field ... experience/ Master's degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience or PhD/PharmD DegreeDegree… more
- Merck & Co. (Rahway, NJ)
- …strategic digital roadmaps, and lead delivery of capital project digital programs.Responsibilities include:Planning and allocating resources for cross-product ... delivery and coordinating with investment Manager to ensure appropriate coordination and forecasting.Communicate IT strategy and portfolio to key stakeholders in our… more
- Merck & Co. (North Wales, PA)
- …writing, and presentation skillsEducation/ExperienceBachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical ... field experience OR Master's Degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD… 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 internal audits and inspections Demonstrate leadership skills via acting as project lead on cross-functional projects in the development and/or implementation of… 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 ... various areas of the business Demonstrate leadership skills via acting as project lead on cross-functional projects in the development and/or implementation of… more
- Merck & Co. (Rahway, NJ)
- … Project management.-Track-record of independent problem-solvingSAP Training and skills - Project Manager (PM) role, SAP Plant Maintenance (Gatekeeping and ... Job DescriptionThis Senior Engineer position will provide engineering support to...of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the formulation… more
- Merck & Co. (North Wales, PA)
- …PowerPoint, Word, Outlook, etc.)Education/ExperienceBachelor's Degree +9 years of pharmaceutical, clinical drug development, project management, and/or medical ... field experienceOR Master's Degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experienceOR PhD/PharmD Degree… more
- Eisai, Inc (Nutley, NJ)
- …Data Review programming and JReview within IODS. Reporting to the Assoc. Director of Clinical Programming is the senior level highly technical SAS and JReview ... is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary: The Senior Director, Head of RBQM (Risk Based Quality Monitoring) sets the vision ... Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves ... as ad hoc member to the Global Project Team for late stage projects. This position manages...technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing… more
- Medix (Grand Rapids, MI)
- …staffing utilization; provide weekly status updates to Site Manager and assigned clinical project manager . Staff Performance & Onboarding: Support the ... and deliver top-tier patient care. We are seeking a Senior Research Nurse to oversee the day-to-day clinical...status updates to Site Manager and assigned clinical project manager . Staff Performance… more
- Genmab (NJ)
- …the above by developing and writing corresponding SAS or other programs. The Senior Programming Manager may also serve as a compound lead.Responsibilities/tasks ... in-house checks of data consistenciesSupports specification and pooling of data across clinical trials within the same project .Supports in-house production of… more
- Merck & Co. (North Wales, PA)
- …with senior cross-functional leadership to optimize efficiencies in the clinical development space. Preferred skills include experience in the application of AI, ... teams both as a direct manager and a second line manager (ie, managers of managers)Demonstrated collaboration with senior cross-functional leadership in… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …daily production schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager , and Manager .Oversee the hiring, development, and ... for overseeing the production of a personalized cell therapy to support both clinical and commercial requirements in either a Grade C or sterile cGMP environment.Key… more
- Commure Athelas (Mountain View, CA)
- …duress alerting, asset tracking, patient elopement, revenue cycle management, clinical documentation and intake, provider copilots, patient engagement and ... execution of all essential aspects of internal operations projects, from project initiation to launch. Engage in cross-functional collaboration with key internal… more
- Alkermes (Waltham, MA)
- Job Description The Senior Manager , Medical Writing, is a key member of the Clinical Development organization responsible for independently authoring, ... managing, and delivering high-quality clinical documents across all phases of development. In addition to hands-on writing, this role provides strategic input into … more
