- 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)
- …and the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs ... distribution- for company development products and non-company marketed products.-Analyzes and anticipates project risks as they relate to clinical supply chain… 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
- Aequor (Thousand Oaks, CA)
- …and education to expanding current job responsibilities. is searching for a Sr. Project Manager in our CMC Integration team within Operation Products Advancement ... main corporate campus in Thousand Oaks, CA. The Sr. Project Manager (PM) will be responsible for...stakeholders, the Sr PM will need to understand the Clinical Development Plan and strategy to enable alignment with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in ... on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking...teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Managed Markets, Legal, Compliance, and Finance. The position has high exposure to senior management and requires a highly motivated individual who is able to work ... of the pharmaceutical marketplace including legal, medical, regulatory and clinical processes Develops accurate short- and long-term plans, forecasting, and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …partners and Promotional Review stakeholders Manage budgets at a project level Physical Requirements 10-20% overnight travel required. Qualifications Bachelor's ... of the pharmaceutical marketplace including legal, medical, regulatory, and clinical processes Ensures timely execution and follow-up, meets deadlines Strong… more
- Merck & Co. (North Wales, PA)
- …is to provide statistical support for the pharmacology components of all clinical trials in our Company's Research Laboratories clinical development pipeline. ... prior to an asset's potential advancement to late stage clinical development are proof of biology/concept clinical ...statistics group to support translational medicine projects as a manager of at least 5 statisticians.Serve as a reviewer… 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
