• Merck & Co. (MA)
    Job DescriptionThe Senior Director ( Sr . Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in… more
    HireLifeScience (10/25/25)
    - Related Jobs
  • Merck & Co. (North Wales, PA)
    …the Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution,-monitoring, analysis, regulatory ... integrating state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director ( Senior Principal Scientist) has primary… more
    HireLifeScience (10/25/25)
    - Related Jobs
  • WCG Clinical (Cary, NC)
    …analysis projects to analyze and interpret statistical data for our clients' clinical study research for potential new medicines. Develop approaches to ... analyses and findings for research protocols or reports. Calculate sample sizes for clinical studies with standard designs and prepare randomization lists, as… more
    DirectEmployers Association (09/26/25)
    - Related Jobs
  • Merck & Co. (South San Francisco, CA)
    …of Phase I studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, ... Job Description Senior Principal Scientist Translational Medicine, Immunology...earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of… more
    HireLifeScience (11/01/25)
    - Related Jobs
  • Merck & Co. (Boston, MA)
    …of external opportunitiesThe Senior Director May: Supervise the execution of clinical studies . Work closely with a cross-functional group of experts in ... Job DescriptionThe Senior Director ( Sr . Principal ...entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation,… more
    HireLifeScience (10/25/25)
    - Related Jobs
  • Merck & Co. (Upper Gwynedd, PA)
    …and programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... Job DescriptionThe Principal Scientist/Director, Value & Implementation (V&I) Outcomes Research,...as well as Outcomes Research.Under the guidance of a senior leader, this position supports value evidence outcomes research… more
    HireLifeScience (10/23/25)
    - Related Jobs
  • Merck & Co. (Rahway, NJ)
    clinical instruction(s) and commercial market approval(s) of combination products. Principal ResponsibilitiesLead, set direction, align with key stakeholders, and ... and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of design… more
    HireLifeScience (10/29/25)
    - Related Jobs
  • Stanford Health Care (Palo Alto, CA)
    …education regarding the clinical trial in the medical record. + Alerts principal investigator of any concerns raised by the patient during the informed consent ... paper if needed) in collaboration with the investigational pharmacy, nursing and principal investigator for therapeutic clinical trials. Assures that the orders… more
    DirectEmployers Association (10/24/25)
    - Related Jobs
  • Merck & Co. (Boston, MA)
    …of Phase I studies ; close collaboration with internal and external clinical study support staff and scientistsProvide clinical pharmacology support ... strategic direction of our Immunology pipeline, building on the Senior Principal Scientist role. This position involves...earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of… more
    HireLifeScience (11/01/25)
    - Related Jobs
  • Arvinas (New Haven, CT)
    …evaluating, and presenting scientific and medical data, writing or providing content to clinical documents ( clinical study protocols and protocol synopses, ... CT, or remote from a location within the US ** Principal Responsibilities** Key responsibilities of this role include, but...Clinical Document Development** + Lead the development of clinical study protocol synopses and full protocols,… more
    DirectEmployers Association (10/28/25)
    - Related Jobs