- Merck & Co. (Boston, MA)
- …Policy to ensure timely and equitable access to our medicines.The Senior Principal Scientist has primary responsibility for protocol development and ... leadership through interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials (design,… more
- Merck & Co. (Rahway, NJ)
- …DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is ... studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and has overall… more
- Merck & Co. (South San Francisco, CA)
- Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... Therapeutic Area Lead in Translational Medicine.Primary responsibilities for the Senior Principal Scientist include the following:Key member of an early… more
- Merck & Co. (South San Francisco, CA)
- …Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking an Associate Principal Scientist to contribute to our Company's biologics, drug ... conjugates, and novel modality discovery and development pipeline. The Associate Principal Scientist will be primarily discovery team-facing and is expected to… more
- Merck & Co. (Boston, MA)
- Job Description Associate Principal Scientist , Protein Engineering, Discovery Biologics We are on a quest for cures and are committed to be the world's premier, ... an energetic and experienced protein engineer for the role of Associate Principal Scientist in the Boston Discovery Biologics group.- They will lead therapeutic… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Principal Scientist , Drug Discovery in our Research and Development Department will be responsible for identifying new molecular entities and ... Safety & Toxicology).- The position will report directly to the Distinguished Scientist and Global Head, our Company's Research & Development Liaison and Discovery… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Microbial Process Operations (MPO) Team is seeking a Senior Principal Scientist with expertise in microbial process development for the ... production of enzymes used in biocatalysis. Our team is part of Continuous & Expression Technologies (CET) within the Process Research & Development - Enabling Technologies (PR&D - ET) group, focused on advancing technologies for the manufacturing of diverse… more
- Merck & Co. (Rahway, NJ)
- Job Description Principal Scientist , Early Development Chemistry, Small Molecule Process R&D Nature and Scope of Position:Reports to the Early Development ... Chemistry Lead within the External Capabilities group of Small Molecule Process R&D, our Research & Development Division . Responsible for the work of teams of scientists at our external partners, the role provides daily scientific oversight and real-time… more
- Merck & Co. (South San Francisco, CA)
- …Sciences (DPS) group based in South San Francisco, CA is seeking an Principal Scientist with small molecule and peptide experience.DPS is a multi-disciplinary ... research group that provides drug delivery, solid state crystal form characterization, pre-formulation and formulation support and small molecule and biologics developability assessments at the development and drug discovery interface. Our team is responsible… more
- Merck & Co. (North Wales, PA)
- …and applying rigorous scientific and ethical standards.The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and ... directing clinical research activities involving new or marketed Neuroscience Medicines. Our company's Neuroscience Medicines span all phases of clinical development (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director… more
- Merck & Co. (MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent… more
- Merck & Co. (South San Francisco, CA)
- …Enabling Capabilities (Analytical R&D) is seeking applicants for an Associate Principal Scientist position available at our research laboratories located ... in South San Francisco, California. The successful candidate must be able to collaborate in a dynamic, integrated, and multidisciplinary team environment. A broad range of tools (eg high-resolution mass spectrometry, chromatography, spectroscopy) are… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Clinical Director ( Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... involving investigational compounds in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent) Our company's Device Product & Process ... and influence clinical and commercial combination product development and launches. Principal ResponsibilitiesLead and set direction for the device development… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionWe are seeking an experienced scientist to join our team and drive innovation in respiratory medicine. The ideal candidate will bring deep expertise ... in respiratory drug development within a large pharmaceutical setting, with a strong track record of advancing programs from early discovery through clinical development. This role offers the opportunity to shape strategy, collaborate across disciplines, and… more
- Merck & Co. (Rahway, NJ)
- …in accordance with regulatory, company, and customer requirements. - Principal Responsibilities Lead/Support continuous improvement initiatives for design control ... and risk management processes Identify and eliminate process inefficiencies using operational excellence tools Develop training materials to foster a culture of operational excellence Ensure processes align with regulatory requirements for medical device and… more
- Merck & Co. (Rahway, NJ)
- …certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for ... annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid… more
- Merck & Co. (North Wales, PA)
- …:Serves as a statistical lead in project teams.Lead, develops, coordinates, and provides biostatistical support for related drug/vaccine projects in Late Development ... Statistics.Lead the interaction with Clinical, Regulatory, Statistical Programming, Data Management, and other Scientists from our Research & Development Division in designing and analyzing clinical trials, and in coordinating the statistical activities for… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic 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)
- …- Under the guidance of dCMC Regulatory-Authoring Leadership, the Associate Principal Scientist , Regulatory Authoring Business Owner, will-optimize regulatory ... authoring processes and enhance data management by working with the business areas to define the optimal route to digitize the authoring of regulatory filing sections.- The applicant will work closely with the cross-functional team to develop and implement the… more
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