- Merck & Co. (San Francisco, CA)
- …Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... Under the broad guidance of the DSCS Digital Program Mgmt Lead, the Associate Director, DSCS Digital Project Manager, will be responsible for implementing… more
- Merck & Co. (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader ... Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD...also be responsible for several effectiveness studies within a project , participating as the clinical representative in… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and ... stages of development therefore requiring someone who has late vaccine clinical development and lifecycle management experience.The AVP will also be responsible… 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 ... will be responsible for implementing new technological solutions for end users.The Associate Director, Clinical Programming manages and oversees JReview and SAS… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Experience Qualifications 7 or More Years of related experience, including Project Management, Clinical Supply Management, and/or Pharmaceutical Development or ... authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the ... size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member...and oversee completion of clinical trial protocols. Provides… more
- Merck & Co. (Rahway, NJ)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck & Co. (Rahway, NJ)
- …the activities of entire Clinical Teams in the execution of clinical studies.--Will report and work collaboratively with the- Associate Vice President to ... commercialization, regulatory affairs, statistics, medical affairs and manufacturing to manage clinical development projects; and assist the Associate Vice… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & ... content strategy and plans with other V&I partners, such as Publications, Clinical and Outcomes Research. Aims to ensure the timely availability of effective… more
- Eisai, Inc (Exton, PA)
- …well as supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing ... your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is...Operations groups to support the supply of DS/ADI for pre- clinical and phase I to phase III clinical… more
- Merck & Co. (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …level handles escalated global CSPV case processing issue and handles project . This position prepares trainings, supports CAPA investigations, case review, ... case processing and related CRO/vendor training needs and reviews case processing project specific training materials. Manages and coaches the PV Vendor Training… more
- Merck & Co. (South San Francisco, CA)
- …Data, AI and Genome Sciences (DAGS)-Department is recruiting-an Associate Director, Computational Biology-in-Cardiometabolic Drug-Discovery-Data Sciences. We are ... data to support drug discovery in the cardiometabolic disease space. The Associate Director will inform discovery, translational medicine, companion diagnostics and … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after ... to external diagnostic business partners specifically:Use of CTA/CDx within clinical trialsDevice protocols and SAPsDevice non-significant/significant risk determinations (both… more
- Merck & Co. (North Wales, PA)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... from data source to analysis/modeling result.Maintain and manage a project plan including resource forecasting.Support the development of programming standards… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves ... as ad hoc member to the Global Project Team for late stage projects. This position manages...technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing… more
- Merck & Co. (Rahway, NJ)
- …build and lead a team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders and key decision makers. ... Development Team, Global Brand and V&I Outcomes Research leads to define clinical development plans and brand strategies for assigned TAsProvides a solid… more
- Merck & Co. (North Wales, PA)
- …and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is responsible and ... President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and direction… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …for overseeing the production of a personalized cell therapy to support both clinical and commercial requirements in either a Grade C or sterile cGMP environment.Key ... execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager, and Manager.Oversee the hiring, development, and… more
