- Bristol Myers Squibb (New Brunswick, NJ)
- …are uncommon in scale and scope. **Job Description:** As a Principal or Senior Principal Scientist in the Drug Product Development - Materials Science ... role may be appointed at the Principal Scientist or Senior Principal Scientist level. Candidates with demonstrated experience and expertise will be… more
- Merck (Rahway, NJ)
- …and Global Policy to ensure timely and equitable access to our medicines. The Senior Principal Scientist has primary responsibility for protocol development ... and external leadership through interaction with key scientific leaders. **Specifically, the Senior Principal Scientist is responsible for:** + Planning… more
- Bristol Myers Squibb (New Brunswick, NJ)
- … Principal Scientist position in the Upstream Process Development team. This Senior Principal Scientist will work with teams across cell line ... development, upstream/downstream process development, and analytical groups to develop efficient and robust upstream processes for BMS's biologics pipeline. Responsibilities include leading a team supporting upstream process development projects, overseeing… more
- Merck (Rahway, NJ)
- **Job Description** **Sr. Principal Scientist - Device Technical and Engineering Lead (Sr. Director Equivalent)** Our company's Device Product & Process ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities:** + Lead and set direction for the device… more
- Merck (Rahway, NJ)
- …and applying rigorous scientific and ethical standards. The Senior Director ( Senior Principal Scientist ) has primary responsibility for the planning ... (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research ... investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development,… more
- Merck (Rahway, NJ)
- …and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of ... clinical instruction(s) and commercial market approval(s) of combination products. ** Principal Responsibilities** + Lead, set direction, align with key stakeholders,… more
- Merck (Rahway, NJ)
- **Job Description** The Principal Scientist , Drug Discovery in our Research and Development Department will be responsible for identifying new molecular entities ... up to the development stage. She/he/they will interface with researchers and senior management throughout the organization as well as external partners and operate… more
- Merck (Rahway, NJ)
- …In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative ... scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of… more
- Merck (Rahway, NJ)
- **Job Description** The **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... and manufacturing to manage clinical development projects + Assist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead in… more
- Merck (Rahway, NJ)
- …& Development, Cell Based Sciences in Rahway, NJ is seeking a motivated senior level scientist with extensive experience in biologics potency assays. More ... specifically, the ideal candidate will be a recognized expert developing mechanism-of-action reflective potency assays for the development of therapeutic proteins, monoclonal antibodies, antibody-drug conjugates, and/or complex modality-based products. **Key… more
- Actalent (Fairfield, NJ)
- Job Title: Experienced Formulation Scientist ( Principal Scientist ) Job Description The Formulation Scientist will be responsible for researching, ... generating, and directing new product formulations from conceptualization through development and manufacture. The role involves collaboration with sales, operations, and quality assurance teams to generate innovative formulations, troubleshoot technical… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development… more
- Bristol Myers Squibb (Madison, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Trial Physician sits within Clinical Development, which is a ... Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management… more
- Bristol Myers Squibb (Madison, NJ)
- …significant, non-significant deviations etc.) * Existing strong relationships with principal investigators. Identifies and cultivates thought leaders in order to ... Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management… more
- J&J Family of Companies (Raritan, NJ)
- …with Cross-Functional Trial Team (CFTT). The SRP provide support to a study senior physician, clinical leader (CL) to deliver a trial(s) in a timely and ... responsible for site interactions in partnership with the clinical project scientist (CPS) for medical questions and education (including safety management… more
- Bristol Myers Squibb (Madison, NJ)
- …on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... lifecycle + Manages site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)… more