- Insmed Incorporated (Bridgewater, NJ)
- …Identifies concerns and champions issue resolution.Oversee medical safety and pharmacovigilance activities conducted in partnership with external business ... Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Executive Director (ED) will provide leadership to the DSPV Medical Safety Team.… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and ... and studies.Adhere to company standards and Research Laboratory/Global Clinical Development (GCD) and GCTO goals, initiatives and expectations.Manage Clinical… more
- Tris Pharma (Monmouth Junction, NJ)
- …privately-owned biopharmaceutical company in the US with a focus on development and commercialization of innovative medicines addressing unmet patient needs. We ... Tris colleagues understand the criticality of operating a successful business and take pride in the company’s success. But...opening in our Monmouth Junction, NJ facility for a Director , Drug Safety. The Director , Drug Safety… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the end-to-end delivery of ... Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and External Vendors for the data services they provide to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Area; Reviews content to be shared with KOLs; Frequent involvement in Business Development activities for late-stage compounds; Involvement with in-licensing and ... and regulatory strategy in collaboration with Regulatory Affairs; Drafts clinical development plans, protocol profiles and sections of key submission documents;… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to providing medical education and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps us all marching to the ... training for Patient Safety (PS) employees' onboarding and on-the-job training for pharmacovigilance as well as Safety training conducted for internal and external… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …suppliers and corporate partners to ensure compliance with SDEA requirements Supports development and maintenance of Pharmacovigilance System Master File (PSMF). ... to providing medical education and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps us all marching to the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and ... innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled Terminology… more
- Ascendis Pharma (Palo Alto, CA)
- …You will be joining the Product Team in Global IT that supports our Pharmacovigilance business function. As IT system manager, you will be supporting Ascendis ... Deep business process knowledge in either Quality, Regulatory or Pharmacovigilance . . Strong configuration skills . Extensive experience with GxP validation such… more
- Taiho Oncology (Princeton, NJ)
- …an Associate Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a dynamic and collaborative environment where your expertise and ... Associate Director , PV Sciences Pleasanton, CA, USA * Princeton,...development /maintenance of Risk Management Plans (RMP) and associated pharmacovigilance and risk minimization activities for team's assigned products.… more
- Lundbeck (Deerfield, IL)
- …and ability to apply concepts of legal/regulatory requirements and guidelines to the pharmacovigilance business . + Advanced ability to develop aggregate data and ... Director Safety Surveillance US - Remote Opportunity Requisition...strategies + Utilizes subject matter expertise to further the development of pharmacovigilance science by staying abreast… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …arrangements with external service providers and partner companies. **Due Diligence, Business Development & Alliance Projects** + Participate, conduct and ... best of my knowledge. **Job Description** **Job Description for Senior Medical Director , Clinical Science, Marketed Products Development ** As the Senior Medical… more
- BeiGene (San Mateo, CA)
- …evaluation/safety monitoring activities and contributes and assists in pharmacovigilance activities including benefit/risk and regulatory activities and ... meetings + Communicate relevant safety information to core team, business partners, and key stakeholders in a timely manner...key stakeholders in a timely manner + Lead the development , update, and review of safety communication documents (eg,… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- Job Title Senior Director , Clinical Development & Medical Affairs (CDMA) Requisition JR000014103 Senior Director , Clinical Development & Medical Affairs ... Headquarters - USA501 Additional Locations Bridgewater, NJ Job Description The Senior Director , Clinical Development Medical Affairs (CDMA) drives strategy and… more
- J&J Family of Companies (Titusville, NJ)
- Director , Medical Safety Officer, Oncology - 2406185159W **Description** Johnson & Johnson, is recruiting for a Director , Medical Safety Officer, Oncology to be ... benefit/risk. The MSO will report to the GMS Sr. Director Product Safety Head, Oncology and oversee the safety...the Oncology TA that are marketed and/or in clinical development . Collaborating with relevant functions, the MSO will ensure… more
- AbbVie (North Chicago, IL)
- …or lead clinical development contributions to due diligence or other business development activity. As required by program needs, contributes in partnership ... Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall… more
- BeiGene (San Mateo, CA)
- …Assurance. This position will be primarily responsible for ensuring research and development , pharmacovigilance and GLP activities are conducted in accordance ... **General Description:** The Director GCP/GLP/GVP Systems & Data Integrity, is responsible...environment **Significant Contacts** + Quality + Clinical Operations + Pharmacovigilance + Clinical Business Operations + Biometrics… more
- Colgate-Palmolive (New York, NY)
- …person is also responsible for driving consumer satisfaction and loyalty to help drive business growth. The Director of NA Operations must have highly developed ... reason to smile and join our global team! The Director of North America (NA) Consumer Care & Experience...loyalty and satisfaction. + Internal expert for Quality, Global Pharmacovigilance , Customer Development , Legal, Risk Management, Colgate… more
- Lilly (Indianapolis, IN)
- …evaluation plan with partners [device safety physician, device surveillance senior/executive director , team members, and internal business partners such as ... experience or experience in areas relevant to drug discovery or development , eg epidemiology, toxicology, pharmacovigilance , regulatory affairs + Experience… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Associate Director , External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process requirement ... research and external connections to work with Corporate and Local Clinical Development and Medical Affairs (CDMA), Legal and other internal partners to process… more
