- J&J Family of Companies (Titusville, NJ)
- …America, Titusville, New Jersey, United States of America **Job Description:** **Senior Manager/Associate Director , Regulatory Medical Writing X-TA** At ... the best talent for a **Senior Manager** **/Associate Director ** , ** Regulatory Medical Writing ** within our Integrated Data Analytics & Reporting (IDAR)… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director or ... for projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory strategy for… more
- Bristol Myers Squibb (Princeton, NJ)
- …and advocating for BMS's position externally. As part of the team, the Associate Director Regulatory Policy brings an expertise in regulatory affairs and ... related policy. The Associate Director , Regulatory Policy is responsible for driving regulatory policy mapping, advocacy, clear objectives and actionable… more
- American Water (Camden, NJ)
- …* Experience in matrixed multi-state utility strongly preferred. * Experience writing and supporting testimony in regulatory proceedings, including live ... package including 401(k),Defined Contribution Plan, Employee Stock Purchase Plan, medical , prescription, dental and vision coverage, plus disability, paid time… more
- Sanofi Group (Morristown, NJ)
- …aim to gain regulatory approval of therapeutic indications. + Coordinate medical writing activities in study teams, including external services. Ensure ... **Job Title:** Associate Director -Principal Medical Writer **Location:** USA, Remote....plans to ensure adequate planning of medical writing activities. Advise team members of regulatory … more
- Sanofi Group (Morristown, NJ)
- …could be critical in helping our teams accelerate progress. **Our Team:** Global Medical writing and Document management serves to generate timely, high quality, ... **Job title:** Associate Director - Principal Medical Writer **Location:**...synergize and harness evolving technologies pushing the edge of regulatory writing . We are an innovative global… more
- Bristol Myers Squibb (Princeton, NJ)
- …RayzeBio aims to be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has responsibility ... treatment of solid tumors, with a focus on GU cancers. This role provides medical direction and high quality scientific and clinical knowledge to lead the strategy… more
- Sumitomo Pharma (Trenton, NJ)
- …. Job Overview The Director , Medical Strategy ... (Prostate Cancer) will be a key member of the Medical Affairs team reporting to the Senior Director...track record of detailed, medically accurate, and scientifically relevant writing and review skills in line with compliance requirements.… more
- J&J Family of Companies (Raritan, NJ)
- …work experience is required. + A minimum of 6 years of direct regulatory labeling content experience developing and writing labeling content for pharmaceutical ... is preferred. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance, etc.) is required.… more
- J&J Family of Companies (Titusville, NJ)
- …quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management, medical writing , biostatistics, ... **We are searching for the best talent for a Director , Clinical Project Physician - Neuropsychiatry.** **POSITION SUMMARY:** **The Project… more