- Merck & Co. (Rahway, NJ)
- …Inventory Management Section of the GCS Planning organization.- Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) ... chain across the full company Research Laboratories portfolio of clinical trials . GCS is accountable for the...activities include, but are not limited to:--Participates on the Clinical Trial Team (CTT) and collaborates closely… more
- Merck & Co. (Rahway, NJ)
- …and the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs ... chain across the full company Research Laboratories portfolio of clinical trials .- GCS is accountable for the...spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related… 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 ... chain across the full company Research Laboratories portfolio of clinical trials .- GCS is accountable for the... Management Skills: strong knowledge of the principles of project management and clinical customer relationship management.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …support training and ensure implementation of ADaM and TLFs standard in clinical trials analysis- Provide programming support to prepare regulatory requested ... proven experience within pharmaceutical industry, or CROs supporting statistical analysis of clinical trials programming with a masters degree required- 3+ Years… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within...other vendor performance against project goals and milestones to monitor and ensure compliance… more
- Genmab (NJ)
- …in-house checks of data consistenciesSupports specification and pooling of data across clinical trials within the same project .Supports in-house production ... listings, and figures)(Preferred) Practical knowledge and experience using R to support clinical trial analyses.About YouYou are genuinely passionate about our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and standards. This position ensures quality delivery of laboratory data for clinical trials , clinical development, and regulatory submissions. This ... develops and proposes strategies for laboratory data ensuring all clinical trials meets quality requirements and best...expertise to promote and implement best practices across the Clinical Trial lifecycle.- Applies GCP principles to… more
- Genmab (NJ)
- …accountable for driving the strategy, quality, and integrity of external data across the clinical trial portfolio. This role serves as a Subject Matter Expert ... to interpret discrepancies and resolve data issues.Cross-functional CollaborationCollaborate with Trial Management, Clinical Operations, Medical, Biomarker Management,… more
- Eisai, Inc (Nutley, NJ)
- … and drug development plans within the clinical development. Works with the clinical , project management, and data manager teams on strategic designs of ... clinical development in that he/she will be responsible for designing clinical trial , performing data analysis, supporting regulatory interactions, overseeing… more
- Genmab (NJ)
- …(eg competitive landscape) that represent operational risks for the execution of clinical trials within the given indication/program.Key contributor to the ... of all aspects of clinical drug development, with particular emphasis on clinical trial design, trial execution, and strong knowledge about the… more
