Regulatory Affairs Intern

2 weeks ago


Jersey City, United States Noven Pharmaceuticals Full time

Overview:

Undergraduate or Graduate student in a Science discipline. This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group. He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. Additionally, the intern will have an opportunity to learn from and work with other functions within Product Development, such as Pharmacovigilance, Clinical Development and Medical Affairs to work on ad hoc projects and understand the roles of these functions within pharmaceutical industry. For this internship opportunity, we are looking for a bright, curious individual, with excellent work ethic, strong attention to detail and a passion to learn about the industry. Ideally, the candidate will have a strong interest in learning about Regulatory Affairs or is, perhaps contemplating a career in Regulatory Affairs within the pharmaceutical industry. Effective written and oral communication skills are important, along with the ability to interact successfully with your supervisor and associates in varied areas of expertise. This will be a rewarding internship experience and great learning opportunity.

Along with your curriculum vitae, please also provide your responses to the Intern Program (IP) application questions. You must be available for the entire internship period (summer and no more than 90 days) and not have conflicting commitments (i.e. rotations, other employment) during that time.

Relocation and housing costs will not be reimbursed.



  • Jersey City, New Jersey, United States Noven Pharmaceuticals Full time

    Overview: Undergraduate or Graduate student in a Science discipline.  This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group.  He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. ...


  • Daly City, United States CareerBuilder Full time

    Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products' registration. Participate on product development teams, providing regulatory strategies, timelines, and direction. Reviews and approves technical documentation....


  • Jersey City, NJ, United States Jefferies Financial Group Full time

    Regulatory Affairs SpecialistPosition This hire will be a member of the Firm’s Regulatory group which is responsible for exam oversight, branch inspections, regulatory change tracking, governance related tasks and additional ad-hoc tasks.  The Firm’s Regulatory Group is housed within its Legal Department.  While attorneys are encouraged to apply,...


  • Oklahoma City, United States Disc Medicine Full time

    Disc Medicine is seeking a Director, Regulatory Affairs-CMC to serve as the Regulatory-CMC lead for Disc Medicine’s small molecule program pipeline. This position will have close collaboration with the development teams and visibility to the executive leadership with meaningful opportunities for professional development and career growth.The position...


  • Redwood City, United States Meet Full time

    Senior Director, Regulatory Affairs (Generalist)Hybrid Role - 3 Days in Menlo Park, CAMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC...


  • Foster City, California, United States Gilead Sciences, Inc. Full time

    Head of CMC Regulatory Affairs Small MoleculesUnited States - California - Foster CityGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living...


  • Oklahoma City, United States HireMinds Full time

    Our cutting-edge, vaccine client is seeking a Sr. Director, Regulatory Affairs (REMOTE) to their growing team! This role will be accountable for developing regulatory strategies for their vaccine candidates with an emphasis on European requirements for early and late-stage assets. This person will be a key regulatory leader who partners with internal and...


  • Oklahoma City, United States EPM Scientific Full time

    Title: Associate Director, Regulatory Affairs Advertising & Promotion The Associate Director, Regulatory Affairs Advertising & Promotion will be responsible for providing strategic, operational and tactical regulatory advice to internal stakeholders regarding communications about investigational product pipeline assets and approved prescription products...

  • Sr. Manager

    1 week ago


    New Jersey, United States Atlas Search Full time

    About the OpportunityOur client is a growing biopharmaceutical company in need of a Sr. Manager/Associate Director of Regulatory Affairs Strategy to join their team. This role is responsible for developing, implementing, and leading short/long term global regulatory strategies that support the success of their pharmaceutical products.The annual base salary...


  • Foster City, California, United States Gilead Sciences, Inc. Full time

    Sr Director, CMC Regulatory Affairs Small MoleculesUnited States - California - Foster CityGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients...


  • Foster City, California, United States Gilead Sciences, Inc. Full time

    Sr Director, CMC Regulatory Affairs Small MoleculesUnited States - California - Foster CityGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients...


  • Foster City, United States Mirum Pharmaceuticals Full time

    If you are not local to the Foster City area, are you willing to relocate? * Yes No I am local Are you currently authorized to work for any employer in the US without visa support? * -- By participating in job interviews, you agree to treat all information shared regarding Mirum’s commercial performance, clinical and scientific data, sensitive corporate...


  • Jersey City, United States Mitsubishi Tanabe Pharma Full time

    Overview: **Entrepreneurial Spirit, Rooted in Tradition**. Mitsubishi Tanabe Pharma America, Inc. (MTPA) is a U.S. subsidiary of Mitsubishi Tanabe Pharma Corporation (MTPC) in Japan, which touts a storied reputation more than 300 years in the making. Our parent company - one of Japan’s most respected - is a research-driven pharmaceutical company that has...


  • Foster City, California, United States Gilead Sciences, Inc. Full time

    Senior Manager, Regulatory Affairs Vendor GovernanceUnited States - California - Foster CityUnited States – RemoteGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve...


  • Jersey City, New Jersey, United States Royal Bank of Canada Full time

    Come Work with UsAt RBC, our culture is deeply supportive and rich in opportunity and reward. You will help our clients thrive and our communities prosper, empowered by a spirit of shared purpose.Whether you're helping clients find new opportunities, developing new technology, or providing expert advice to internal partners, you will be doing work that...


  • Foster City, California, United States Gilead Sciences, Inc. Full time

    Associate Director, Regulatory Affairs Advertising and PromotionUnited States - California - Foster CityGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of...


  • Foster City, California, United States Gilead Sciences, Inc. Full time

    Associate Director, Regulatory Affairs Advertising and PromotionUnited States - California - Foster CityUnited States - New Jersey - ParsippanyGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug...


  • Florham Park, New Jersey, United States AbbVie Full time

    Job Description *Position can sit in our Lake County, IL or Madison, NJ offices. The Scientific Director for US Medical Affairs in CNS/Psychiatry provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; evidence generation of clinical and...


  • Foster City, United States Mirum Pharmaceuticals Inc Full time

    MISSION Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases affecting children and adults. Propelled by our passion for patients and their families, we're focused on turning possibilities into realities. Using data and meaningful evidence, our goal is to transform scientific discoveries into...


  • Florham Park, New Jersey, United States AbbVie Full time

    Job Description Provides medical, scientific, strategic and operational leadership and expertise into core medical affairs activities such as: generation of clinical and scientific data) (enhancing therapeutic benefit, safety, and value) health-care professional and provider collaborations and interactions;); medical education, scientific communications...