- 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 Operations, in ... This may include preparing meeting logistics, distributing agendas, and minutes for study team meeting, meetings with Academic Research Organizations (AROs), and… more
- Merck & Co. (San Francisco, CA)
- …talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration. Associate Directors are emerging leaders in the field of quantitative drug… more
- Merck & Co. (Rahway, NJ)
- …Practice (GLP) studies .The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study .The ... Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD... protocol/related documentation.Provide overall leadership and support to the study team . Identify and select Investigators, laboratories… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …contact for the assigned studies and projects. Provides guidance to study team on all aspects of statistical activities; collaborates closely with ... rare diseases and immune disorders. Job Summary: Position leads complex studies in study design, statistical analysis and interpretation of results with some… more
- Aequor (Thousand Oaks, CA)
- Fully remote MCS Supply Chain Sr Associate Ideal candidate: Experience is document management. Very document orientation and detail oriented Description: Reports to ... to support inspection readiness for various clinical programs and clinical studies . Key Responsibilities: Inspection Readiness for clinical programs and studies… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The RoleThe Associate Director, External Data Quality Management, is a strategic leadership role within Clinical ... for inspection readiness, regulatory compliance, and successful data submissions.The Associate Director will lead cross-functional collaboration, provide oversight of… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the ... technical skills in SAS systems and application development and experience. The Associate Director must be a highly specialized individual contributor or functional… more
- Genmab (NJ)
- …final operational plan approval and final feasibility. KPIs developed and shared across the study team as part of year end objectives.Point of contact for ... and development of data-driven early indication and program assessments, study -level feasibility assessments, robust country and site identification, support of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and ... to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the strategic direction to Biostatistics Data… more
- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and ... building a scientific team focused on the technology transfer, scale-up, and optimization...supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing… more
