• Insmed Incorporated (NJ)
    …to the Head of Scientific Communications & Publications, you'll lead the development and implementation of global Medical Communications Strategy across regions. You ... in a matrixed organization. A core responsibility will be to co-lead the development and maintenance of scientific platforms and the strategic execution of aligned… more
    HireLifeScience (11/22/25)
    - Related Jobs
  • Merck & Co. (Rahway, NJ)
    …which includes Global Medical and Scientific Affairs as well as Outcomes Research . This position executes the patient engagement strategy in alignment with our ... health, public policy, epidemiology, or other relevant degree required; MD, PhD , NP, PharmD or equivalentRequired Experience and Skills:Deep academic understanding… more
    HireLifeScience (11/21/25)
    - Related Jobs
  • Genmab (NJ)
    …initiatives. They will compliantly partner with both CORE (Center for Outcomes Research , Real-world evidence, and Epidemiology) and US Market Access leadership teams ... in the field, providing the HEOLs with an individualized view of their development plans and ongoing performance. This is a remote position (field-based). Domestic… more
    HireLifeScience (10/21/25)
    - Related Jobs
  • Parexel (Trenton, NJ)
    …clearly describe advanced statistical techniques and interpret results + Familiarity with regulatory / research guidelines on drug development , GCP, and ... to work independently + Good mentoring/leadership skills + Good business awareness/ business development **Knowledge and Experience** : + PhD or MS in Statistics… more
    DirectEmployers Association (11/21/25)
    - Related Jobs
  • Organon & Co. (Jersey City, NJ)
    …Assessment Lead will oversee non-clinical activities and safety assessments for Organon Research and Development (R&D) programs ranging from discovery through ... development strategy. Additionally, cross-functional interactions with early clinical development , late-clinical development , regulatory affairs, safety… more
    DirectEmployers Association (11/18/25)
    - Related Jobs
  • Terumo Medical Corporation (Somerset, NJ)
    …in the clinical research and participate in investigator launch meetings. + Regulatory activities partnership: + Work with regulatory affairs to ensure that ... the organization that includes Medical Affairs, Clinical Operations, Sales, Marketing, Regulatory Affairs, to ensure maximum exchange of information and insights.… more
    DirectEmployers Association (10/01/25)
    - Related Jobs
  • Organon & Co. (Jersey City, NJ)
    …knowledge-sharing events. + Contribute to and/or review the nonclinical, early clinical development or CMC documentation to support regulatory or other ... of drug candidates. + Working knowledge of early clinical development and clinical pharmacology-, modeling- and bioanalytical-related regulatory guidelines… more
    DirectEmployers Association (10/24/25)
    - Related Jobs
  • Terumo Medical Corporation (Somerset, NJ)
    …of research , the Sr. Medical Writer will support the development and creation of clinical and scientific documents to present information effectively, ... content for scientific presentations preferred . + Demonstrated experience in the development of regulatory /clinical submissions, preferably as a medical writer… more
    DirectEmployers Association (10/21/25)
    - Related Jobs
  • Sun Pharmaceuticals, Inc (Princeton, NJ)
    …impacts. + Lead through Internal Collaboration: Forge strong collaborations with clinical development , medical affairs, and regulatory teams to ensure seamless ... have access to Suns medicines. **Duties and responsibilities** + Lead the Development and Implementation of Innovative Access Strategies: Lead the development more
    DirectEmployers Association (09/24/25)
    - Related Jobs
  • Summer Intern PhD Student - Chemical…

    Bristol Myers Squibb (New Brunswick, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Chemical Process Development (CPD) is a team of organic chemists, analytical chemists, and ... the manufacturing process, design parameters, and control strategies enables regulatory filings to bring these novel medicines to patients...work with mentors for ~10 weeks on a guided research project within a CPD Project Team. The program… more
    Bristol Myers Squibb (11/08/25)
    - Related Jobs