Current jobs related to Sr / Manager, Regulatory Affairs (Strategy) - Florham Park - Planet Pharma

  • Senior Manager, Regulatory Affairs Strategy

    3 weeks ago

    Florham Park, United States Planet Pharma Full time

    OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior Director in overseeing regulatory activities related to QOL initiatives. This role involves actively contributing to the development and execution of regulatory strategies, regulatory submissions, and collaboration with regional...

  • Regulatory Affairs Manager

    3 weeks ago

    Florham Park, United States Planet Pharma Full time

    Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

  • Regulatory Affairs Manager

    3 weeks ago

    Florham Park, United States Planet Pharma Full time

    Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

  • Regulatory Affairs Manager

    3 weeks ago

    florham park, United States Planet Pharma Full time

    Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

  • Regulatory Affairs Manager

    2 weeks ago

    florham park, United States Planet Pharma Full time

    Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

  • Regulatory Affairs Specialist

    2 weeks ago

    Florham Park, New Jersey, United States Planet Pharma Full time

    Job Title: Regulatory Affairs ManagerPlanet Pharma is seeking a highly skilled Regulatory Affairs Manager to support the development and execution of regulatory strategies for our quality-of-life initiatives.Key Responsibilities:Develop and execute regional regulatory strategies for quality-of-life initiatives.Provide strategic oversight and leadership to...

  • Regulatory Affairs Director

    2 weeks ago

    Florham Park, New Jersey, United States Planet Pharma Full time

    Job Title: Associate Director, Regulatory Affairs - GDP ContractorFlorham Park, NJ - Onsite 2-3x a week1-year contract with potential to extendJob Summary:The Associate Director, Regulatory Affairs - GDP Contractor, plays a pivotal role in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves...

  • Regulatory Affairs Specialist

    2 weeks ago

    Baldwin Park, California, United States Ihealth Labs Inc Full time

    Job Title: Sr. Regulatory Affairs SpecialistJoin iHealth Labs Inc, a leading provider of cloud-connected medical devices, personal health care devices, and home-based tests, as a Sr. Regulatory Affairs Specialist. In this role, you will be part of the regulatory team responsible for proper oversight of medical device development and market introduction.Key...

  • Regulatory Affairs Director

    2 weeks ago

    Florham Park, New Jersey, United States Shionogi Inc. Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Director to join our team at Shionogi Inc. This role will provide essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale.Key ResponsibilitiesDevelop and execute regional regulatory strategies for antiviral...

  • Regulatory Affairs Director

    4 weeks ago

    Florham Park, New Jersey, United States AbbVie Full time

    Job DescriptionAbbVie is seeking a highly skilled and experienced Regulatory Affairs Director to join our Global Regulatory Strategy team. As a key member of our team, you will be responsible for developing and implementing global regulatory strategies to secure and maintain market approval for our products.The ideal candidate will have a strong...

  • Regulatory Affairs Specialist

    3 weeks ago

    Baldwin Park, California, United States Ihealth Labs Inc Full time

    Job Title: Sr. Regulatory Affairs SpecialistJoin iHealth Labs Inc, a leading provider of cloud-connected medical devices, personal health care devices, and home-based tests, as a Sr. Regulatory Affairs Specialist. In this role, you will be part of the regulatory team responsible for proper oversight of medical device development and market introduction.Key...

  • AD/Director Regulatory Affairs, GDP

    2 weeks ago

    florham park, United States Planet Pharma Full time

    Florham Park, NJ- onsite 2-3x a week1 year contract with potential to extendOverview:The Associate Director, Regulatory Affairs – GDP Contractor, provides essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves assisting in the development and...

  • AD/Director Regulatory Affairs, GDP

    4 weeks ago

    Florham Park, United States Planet Pharma Full time

    Florham Park, NJ- onsite 2-3x a week1 year contract with potential to extendOverview:The Associate Director, Regulatory Affairs – GDP Contractor, provides essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves assisting in the development and...

  • Sr. Regulatory Affairs Specialist

    2 weeks ago

    Baldwin Park, United States Ihealth Labs Inc Full time

    Job DescriptionJob DescriptionWork Location: Irwindale, CaliforniaSalary Range: $80,000 - $140,000 depending on related working experienceJob Type: Full-Time OnsiteOur Company:Founded in 2010, iHealth Labs is dedicated to empowering people to live healthier lives. The company is a leading provider of cloud-connected medical devices, personal health care...

  • Associate Director/Director, Regulatory Affairs

    8 hours ago

    Florham Park, United States Shionogi Inc. Full time

    Overview The Associate Director/Director, Regulatory Affairs - Global Development Products (Anti-Viral), provides essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves assisting in the development and execution of regulatory strategies, regulatory...

  • Medical Director/Scientific Director, Medical Affairs

    2 weeks ago

    Florham Park, New Jersey, United States AbbVie Full time

    Job DescriptionAbbVie is seeking a highly skilled Medical Director/Scientific Director to join our Medical Affairs team. As a key member of our team, you will provide strategic medical and scientific input into core medical affairs activities, including health-care professional and provider interactions, generation of clinical and scientific data,...

  • Regulatory Affairs Specialist

    2 weeks ago

    Menlo Park, California, United States Katalyst Healthcares & Life Sciences Full time

    Key Responsibilities:As a Regulatory Affairs Specialist at Katalyst Healthcares & Life Sciences, you will be responsible for managing the company's regulatory interface with domestic and international health authorities. This includes developing and deploying the regulatory program to ensure aggressive product approval. You will also manage and generate...

  • Medical Director/Scientific Director, Medical Affairs

    2 weeks ago

    Florham Park, New Jersey, United States AbbVie Full time

    Job DescriptionAbbVie is seeking a highly skilled Medical Director/Scientific Director to join our Medical Affairs team. As a key member of our team, you will provide strategic medical and scientific input into core medical affairs activities, including health-care professional and provider interactions, generation of clinical and scientific data,...

  • Medical Director, Medical Affairs

    1 week ago

    Florham Park, New Jersey, United States AbbVie Full time

    Job SummaryAbbVie is seeking a highly skilled Medical Director, Medical Affairs to provide strategic and operational input into core medical affairs activities. The ideal candidate will have a strong understanding of relevant therapeutic areas and experience in generating clinical and scientific data.Key Responsibilities:Contribute to the development of...

  • Medical Director, Medical Affairs

    4 weeks ago

    Florham Park, New Jersey, United States AbbVie Full time

    Job SummaryAbbVie is seeking a highly skilled Medical Director or Scientific Director to join our Medical Affairs team. As a key member of our team, you will be responsible for providing strategic medical and scientific input into core medical affairs activities, including healthcare professional/provider interactions, generation of clinical and scientific...

Sr / Manager, Regulatory Affairs (Strategy)

3 months ago

Florham Park, United States Planet Pharma Full time

Please apply if you think you are a good fit for the following:


  • MUST have at least 5 yrs of REGULATORY STRATEGY experience
  • Experience with IND submissions, preparing for meetings and briefing documents and FDA documents.
  • IND; phase 1 and 2; Marketed products
  • Dynamic fast paced environment
  • TA; Anti viral, infectious disease, obesity drug, RSV; Any TA background will work