- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in the absence of Asset Lead).-Where appropriate, may delegate certain responsibilities to Study Manager (s) assigned to the study - Protocol Development, and ... areas centered around rare diseases and immune disorders. SummaryThe Study Delivery Lead (SDL) leads the cross functional core...SDL has the accountability for 1 or several complex studies in various settings including Phase I-III, within a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in planning and execution of clinical studies , under the supervision of the Study Manager role the Study Associate Manager within Clinical ... archive. Bring issues with the reconciliation to the attention of the Study Manager and propose remediation plan.Distribute key study documents to the… more
- BeOne Medicines (San Mateo, CA)
- …updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional study team at ... Study Report in collaboration with Global Clinical Study Manager and Medical Writing **Quality:** +...and the quality of the work performed on assigned studies + Contributes to development, optimization and review of… more
- Aequor (Basking Ridge, NJ)
- Duties: Participate in study team meeting, align with study details and collaborate in meeting study objective, Provide supporting information to the teams, ... Create drug supply forecast for packaging and labeling operations. Support patient study needs that consider enrollment rates, country logistics for shipping and… more
- Insmed Incorporated (NJ)
- …for the future of science, we're in. Are you?About the Role:The Clinical Trial Manager will be responsible for the management and oversight of phase I-IV clinical ... limited to, development of project documentation, training project staff, monitoring study progress, assessing protocol adherence, administration and oversight of … more
- BeOne Medicines (San Mateo, CA)
- …management responsibilities:_ + Provides leadership, management, and/or mentorship to clinical study managers at various levels for assigned portfolio + Collaborates ... metrics + Contributes to resourcing and capability development related to regional study management + Ensures alignment of regional resources and deliverables with… more
- Genmab (NJ)
- …a fit? Then we would love to have you join us!The RoleThe Senior Manager , Clinical Programming is responsible for the establishment, governance, and integrity of ... Study Data Tabulation Model (SDTM) standards, perform sponsor oversight...across programs and systems. Responsibilities Develops and implements company Study Data Tabulation Model (SDTM) standards that support the… more
- Eisai, Inc (Nutley, NJ)
- …to hear from you. Responsible for SAS programming activities supporting multiple studies for a single, or multiple compounds within related therapeutic areas. ... Programming experience from inception through submission in related areas.Senior Manager , Statistical Programming sought by Eisai Inc. in Nutley, NJ. Responsible for… more
- BioAgilytix (San Diego, CA)
- …you enable life-changing, life-saving therapeutics to the patients who need them.The Manager II will lead scientific and operational activities in support of ... preclinical, clinical, and product release studies for our San Diego lab. This role requires...reports and prepare SOPs.Fulfill the role of Bioanalytical Project Manager (BPM)/Principal Investigator (PI) for all assigned clients and… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. The Manager Product training is responsible for the following:- Developing and implementing training programs ... program. Responsibilities: Develop, coordinate and deliver live/virtual new hire home study and resource prep training on disease state, product knowledge and… more
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