- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and control of Clinical Project Budget in support of Phase I-III clinical studies . Partner with Project Management , Clinical Operations and other functional ... planning, internal reporting, ad hoc reporting and analysis, and change management initiatives. Also responsible for expense or headcount control procedures and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …service types, studies , and programs- Responsible for the development and management of other ad hoc special projects as they arise through minimal supervision. ... plans for specific categories under the direction of the head of category management , for the creation, execution, tracking of strategies. Includes working under a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders. Summary A key part of the Global HR team, the Associate Director of Global HR Communications and Change Management will be responsible for ... but are not limited to, global job grading structure, global performance management , global HRIS, global culture initiatives, and global reorganization. This role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global ... International Conference on Harmonization (ICH) guidelines. This role emphasizes the management of Investigator Initiated Studies (IIS) and Collaborative… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … from end to end in collaboration with GCLs, Physician Scientists and the study team (data management , clinical operation and other functions) to implement ... for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical Science (CS) Group Lead will… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 -… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the internal and external network, Manages Phase 1 -… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …major milestones of trial, clinical trial plan and contingency planning, Analyzes, updates management on potential risks to study deliverables, Provides input on ... PIs to plan study and monitor completionStudy outputs: For Phase 2 studies : Drafts responses to IRBs and HA, Collaborates with TMCP to ensure appropriate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …major milestones of trial, clinical trial plan and contingency planning, Analyzes, updates management on potential risks to study deliverables, provides input on ... for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO; Participates in creation of...and PIs to plan study and monitor completion. Study outputs: For Phase 2 studies : Drafts… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …interpret Phase 1 (specifically Clinical Pharmacology) studies , support Phase 2/3 studies , represent function on study and project teams, and participate in ... functions as Study Team Leader for Phase 1 Clinical Pharmacology studies , and provides clinical pharmacology input and support for other phase 1-4 clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies , conduct hands on ... opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing Clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …indications.Serve as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document ... other research areas centered around rare diseases and immune disorders. Summary The Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the… more
- Tris Pharma (Monmouth Junction, NJ)
- Associate Director / Director , Analytical Research and DevelopmentMonmouth Junction, NJ Analytical Development, R&DDescriptionTris Pharma, Inc. ... Junction, NJ headquarters has an immediate need for an experienced Associate Director / Director , Analytical Research & Development. Job Title commensurate with… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …gene therapy. Experience with in vivo CAR-T and preclinical studies . Excellent leadership, communication, and project management skills.#LI-LB1#LI-OnsiteLegend ... in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team based in… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …acting as an internal subject matter expert and limited scope client interaction to assist management or director study with execution or resolution of ... complex laboratory duties. The Laboratory Supervisor will organize and coordinate studies in addition to documenting laboratory work and maintaining laboratory… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for assigned compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical Affairs (USOMA). Develops ... activities in the USOMA plan including Launch Readiness and Life Cycle Management . Leads the team for this compound.Responsibilities- Responsible for the development… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility to lead ... monitoring and oversight of assigned clinical programs including monitoring of clinical studies , review & interpretation of clinical trial data, authoring clinical … more
- Merck & Co. (North Wales, PA)
- …internal teams and external partners, design non-interventional and data synthesis studies , author study protocols, develop measurement questionnaires, case ... study reports, scientific presentations, and publications.Responsible for study -related contracting, budgets, and vendor/partner management .Develop American… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …contribute to strategic planning and provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess ... centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for producing scientifically… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …contribute to strategic planning and provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess ... research areas centered around rare diseases and immune disorders.Summary The Associate Director of Regulatory Writing is a key role responsible for producing… more
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