- Aequor (Bothell, WA)
- …SUMMARY:The Downstream Process Development group in Bioprocess R&D is seeking a Senior Associate Scientist contractor to support development and optimization of ... limited to designing and executing bench-scale development and characterization studies with proper documentation, analyzing and interpreting results, and authoring… more
- Aequor (Newbury Park, CA)
- …Regulatory Lead to manage GRT interactions The responsibilities of the Regulatory Affairs Senior Associate position are: Assist US Regulatory Lead to support ... regulatory packages and cross-reference letters to support investigator initiated studies Complete regulatory forms to support agency communications Provide… more
- Genmab (Plainsboro, NJ)
- …and authentic is essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager, you will be in the ... responsibilities include:Supports and/or leads programming efforts within a clinical study , depending on background and experience.As a lead, reviews CRFs… 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 Operations, in ... (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and… more
- Aequor (Thousand Oaks, CA)
- …Anticipates and resolves conflict situations in a win-win outcome. Contributes to study management and the development of study documents as appropriate ... as well as any updates/amendments, ensuring template and version compliance. Manages the set-up of third-party vendors, assessing initial statement of work and budget, as well as the change order process. Prepares presentation material for meetings and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …position, task oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence to Project objectives, ... vendors. Supports regular vendor/sponsor discussions to identify risks and ongoing study support. Identifies critical issues which may compromise patient dosing or… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder the guidance of a senior leader, an Associate Principal Scientist has primary responsibility for planning/managing real world and outcomes ... and outcomes research activities linked to V&I goals.Responsible for study -related contracting, budgets, and vendor/partner management.Support market affiliates to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development,… more
- Merck & Co. (Rahway, NJ)
- …the timely and efficient delivery of the biomarker operational aspects of each study .This position will report into the Associate Principal Scientist of Project ... Job DescriptionWe are currently seeking a Senior Scientist within the Integrated Biomarker Operations organization...specimen collection, testing and data delivery activities in clinical studies . The primary focus of this position is in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Budget; Establishes effective communication between CRO / vendors / AROAdditional non- study related activities: Occasional senior management interactions at ... to Clinical Operations. Represents Clinical Development on Project Teams. Responsibilities Study Strategy: Provides the strategic direction to Biostats Data Mgmt &… more
