- Merck & Co. (Boston, MA)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire ... execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Merck & Co. (Boston, MA)
- …marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area . The Executive Director will manage and oversee the entire ... and will interact externally with key opinion leaders.-Specifically, the Executive Director may be responsible for:Evaluating pre- clinical and translational work… more
- Eisai, Inc (Nutley, NJ)
- …standard macro library, standard listings, and reports.Proactively identify and track Oncology clinical area need in terms of program development and ... profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in...have expertise in addressing technical challenges in the programming area that connect JReview, SAS, EDC, and CDISC standards.… more
- Eisai, Inc (Nutley, NJ)
- …and for-cause audits Knowledge of data integrity controls and systems quality for clinical area Strong analytical skills and report writing skills Experience ... is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director...discipline (advanced degree preferred) with minimum 12 years in clinical research/ operations/ data management or related area… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …managing multiple direct reports. Responsibilities:Operational Strategy:Align with the Head of Clinical Development Operations or Senior Director , Clinical ... Clinical Operations on the Strategy and Portfolio or Clinical Sub Teams in their therapeutic area .Ensure...or Clinical Sub Teams in their therapeutic area .Ensure operational aspects are incorporated into CDP planning and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing,...activities as a subject matter expert in a particular area of expertise.- Mentors new team members and supports… more
- Merck & Co. (North Wales, PA)
- …the Company's Areas of Interest (AOI) for the Regional Medical Scientific Director specific therapeutic area .ResearchUpon request from Global Center for ... Job DescriptionRole SummaryThe Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in… more
- Eisai, Inc (Exton, PA)
- …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 ... new products in development through their lifecycle (Preclinical through phase III clinical development) at the Biologics Pilot Plant as well as supporting… more
- Merck & Co. (Rahway, NJ)
- …to understand our customers' needs and provide solutions to meet their needs.The Director , Global Market Access Oncology, lead the pipeline TROP 2 asset in ... access.The candidate will work closely with value and Implementation teams under clinical development to ensure all clinical trials include the appropriate… more
- Merck & Co. (Rahway, NJ)
- …the guidance of a senior leader, a Senior Principal Scientist/Senior Director , has primary responsibility for developing value evidence strategies, and ... planning/managing real world and economic evidence activities in the opthalmology area to meet the value evidence needs of clinicians, payers, policymakers,… more
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