- Merck & Co. (South San Francisco, CA)
- …group within Data, AI and Genome Sciences (DAGS). Our department is recruiting a Senior Director , who will serve as the Computational Biology lead for ... Cardiometabolic Drug Discovery Data Science. We are seeking an experienced...discovery, translational medicine, companion diagnostics and clinical research. The Senior Director will also serve as a… more
- Merck & Co. (Rahway, NJ)
- …medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development, ... design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director may be responsible for: Providing scientific… more
- Merck & Co. (Upper Gwynedd, PA)
- …create breakthrough science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the ... Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the...decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and participating… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new ... medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical… more
- Eisai, Inc (Nutley, NJ)
- …per week#LI-CCEisai Salary Transparency Language:The base salary range for the Senior Director , Clinical Quality Assurance is from :236,900-310,900Under current ... US FDA, PMDA, ICH, and National regulations).In the current times, drug development is going through a significant transformation with digitalization, utilization… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Project Team (GPT) for any projects that definitively require a CDx for drug registration or for any project with CDPs containing multiple registrational clinical ... submission strategies. May represent DS in various Health Authority interactions for the drug trials or for approval of CDx. Keeps abreast of regulatory and policy… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations staff ... and ensure ongoing collaboration and communication with internal stakeholders. Detailing The Senior Director will ensure a robust communication plan including… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …The position will define and oversee the translational medicine strategy for a drug program across multiple indications. The successful candidate will set goals and ... Lead the Translational Subteam within the Global Project Team for the drug program. Present as needed at internal and external meetings. Qualifications: Successful… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of integrated ... departments to strategically manage benefit-risk throughout the lifecycle of the drug . Specific responsibilities will vary depending on the stage of development… more
- Tris Pharma (Monmouth Junction, NJ)
- …Director / Director , Procurement. Title and salary commensurate with experience. The Director / Senior Director , Procurement is responsible for multiple ... the organization. Ensures compliance with all current GxPs, Food and Drug Administration (FDA), Drug Enforcement Administration (DEA), and Occupational… more
- Merck & Co. (North Wales, PA)
- …of the CIPM Staff Manager & Portfolio Lead, the core responsibility of this senior Project Manager (PM) role will be to manage CMC programs, due diligence and ... supervisors, rather than "oversight" is expected at this level. In addition, the Director may be expected to take on one of the following important responsibilities:… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of...Clinical Development; Must have a strong understanding of pharmaceutical drug development. A background in biologics would be ideal.Must… more
- Merck & Co. (Rahway, NJ)
- …GMP capability build for the production of clinical supplies of bulk biologic drug substance at a state-of-the-art Next Generation Biologics (NGB) facility at our ... 3-4 exempt and non-exempt employees to support bulk clinical manufacturing of biologic drug substances, and at times will require hands-on approach on the processing… more
- Eisai, Inc (Nutley, NJ)
- …to soft skills, business skills, and emotional intelligence d) consistently support senior management decisions and train colleagues and new hires to think ... strategically in an effort to support decisions made by senior management. e) increase the proficiency of the Global & US Medical Affairs colleagues regarding… more
- Merck & Co. (Rahway, NJ)
- Job Description-The Senior Director ( Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving ... cardiovascular and respiratory medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development,… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionThe Executive Director of Metabolism & Obesity will be responsible for overseeing and facilitating the research in metabolic diseases & obesity and ... while focusing on uncovering novel biology that delivers high-quality drug discovery pipeline.-We are a research-driven biopharmaceutical company. -Our mission… more
- Merck & Co. (Rahway, NJ)
- …integrating state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director ( Senior Principal Scientist) has primary ... development (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development,… more
- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career. Senior Director ( Senior Principal Scientist) has primary responsibility ... oncology medicines span all phases of clinical development (pre-clinical to post-licensure).The Senior Director will manage the entire cycle of clinical… more
- Merck & Co. (Rahway, NJ)
- …an experienced leader who will manage a team of scientists to support drug substance process development activities to enable and accelerate early and late-stage ... pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics Process Research and… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
