Regulatory Affairs Director, Precision Medicine

7 days ago


Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

About the Role

Gilead Sciences International, Ltd. is seeking a highly skilled and experienced Director, Global Regulatory Affairs, Precision Medicine to join our team. As a key member of our regulatory affairs department, you will play a critical role in developing and executing precision medicine regulatory strategies in alignment with our global regulatory strategy.

Key Responsibilities

  • Develop and lead precision medicine regulatory strategies to support Gilead assets from early development through registration.
  • Represent Gilead's regulatory affairs expertise on cross-functional teams and present to senior leadership as required.
  • Maintain current understanding of global IVD/CDx regulations and assess their impact on drug and IVD/CDx development and registration activities.
  • Provide regulatory input during clinical development to ensure compliance with global and local regulatory requirements.
  • Lead the preparation and filing of HA briefing books and provide inputs on key development documents.
  • Manage internal and external stakeholders to advance scientific and technical capabilities in precision medicine.
  • Contribute to local and/or global process improvements that have a significant impact on business.
  • Support or lead training related to IVD/CDx development and registration activities.
  • Ensure compliance with established practices, policies, processes, and regulatory requirements.

Requirements

  • BA/BS or advanced degree in life sciences or related field with significant regulatory experience in the biopharma industry, regulatory agency, clinical research, or other related healthcare environment.
  • Demonstrated ability to be a fast learner and flexible in a dynamic environment.
  • Advanced knowledge of regulatory requirements, including those related to IVDs, and the role of regulatory affairs in achieving cross-functional drug discovery and development goals.
  • In-depth knowledge of relevant health authorities and their requirements.
  • Strong analytical thinking skills, attention-to-detail, and communication and writing skills.
  • Ability to lead and influence programs, projects, and initiatives.
  • Strong interpersonal and communication skills with ability to rapidly understand and navigate team dynamics.
  • Proven ability to work successfully in a team-oriented, matrixed environment.

About Gilead Sciences International, Ltd.

Gilead Sciences International, Ltd. is a biopharmaceutical company that discovers, develops, and commercializes innovative therapies for complex, life-threatening diseases. We are committed to making a difference in the lives of patients and communities around the world.



  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Gilead Sciences International, Ltd. is seeking a highly motivated and experienced Director of Global Regulatory Affairs for Precision Medicine to play a pivotal role in shaping the regulatory landscape for our innovative therapies. This position demands a deep understanding of global regulatory requirements, particularly within the dynamic field of...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Gilead Sciences International, Ltd. is seeking a highly motivated and experienced Director of Global Regulatory Affairs for Precision Medicine to play a pivotal role in shaping the regulatory landscape for our innovative therapies. This position demands a deep understanding of global regulatory requirements, particularly within the dynamic field of...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    About the RoleGilead Sciences International, Ltd. is seeking a highly skilled and experienced Director, Global Regulatory Affairs, Precision Medicine to join our team. As a key member of our regulatory affairs department, you will play a critical role in developing and executing precision medicine regulatory strategies in alignment with our global regulatory...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    About the RoleGilead Sciences International, Ltd. is seeking a highly skilled and experienced Director, Global Regulatory Affairs, Precision Medicine to join our team. As a key member of our regulatory affairs department, you will play a critical role in developing and executing precision medicine regulatory strategies in alignment with our global regulatory...


  • Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time

    Job DescriptionJob Title: Director, Global Regulatory Affairs, OncologyJob Summary:We are seeking an experienced and skilled Director, Global Regulatory Affairs, Oncology to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and executing regulatory strategies for our assigned programs and products.Key...


  • Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time

    Job DescriptionJob Title: Director, Global Regulatory Affairs, OncologyJob Summary:We are seeking an experienced and skilled Director, Global Regulatory Affairs, Oncology to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and executing regulatory strategies for our assigned programs and products.Key...


  • Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time

    Job DescriptionJob SummaryWe are seeking a highly experienced Regulatory Affairs Director to lead our global regulatory strategy for oncology products. As a key member of our team, you will be responsible for developing and executing regulatory strategies to ensure compliance with global regulations and to drive business growth.Key ResponsibilitiesRegulatory...


  • Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time

    Job DescriptionJob SummaryWe are seeking a highly experienced Regulatory Affairs Director to lead our global regulatory strategy for oncology products. As a key member of our team, you will be responsible for developing and executing regulatory strategies to ensure compliance with global regulations and to drive business growth.Key ResponsibilitiesRegulatory...


  • Cambridge, Cambridgeshire, United Kingdom Relay Therapeutics Full time

    The Opportunity:We are seeking a seasoned regulatory professional to join our team at Relay Therapeutics as a Director of Regulatory Affairs. As a key member of our regulatory team, you will play a critical role in defining and implementing innovative regulatory strategies to drive the development and approval of our transformative pipeline.Your Role:You...


  • Cambridge, Cambridgeshire, United Kingdom Relay Therapeutics Full time

    The Opportunity:We are seeking a seasoned regulatory professional to join our team at Relay Therapeutics as a Director of Regulatory Affairs. As a key member of our regulatory team, you will play a critical role in shaping and implementing our regulatory strategies to drive the development and approval of our innovative pipeline.Your Role:You will report to...


  • Cambridge, Cambridgeshire, United Kingdom Relay Therapeutics Full time

    The Opportunity:We are seeking a seasoned regulatory professional to join our team at Relay Therapeutics as a Director of Regulatory Affairs. As a key member of our regulatory team, you will play a critical role in shaping and implementing our regulatory strategies to drive the development and approval of our innovative pipeline.Your Role:You will report to...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Gilead Sciences International, Ltd. is seeking a highly motivated and experienced Regulatory Affairs professional to join our global team as an Associate Director, Regulatory Affairs CMC. In this role, you will be responsible for leading the regulatory strategy and submissions for Kite's existing commercial and/or clinical programs within the EU region. You...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Gilead Sciences International, Ltd. is seeking a highly motivated and experienced Regulatory Affairs professional to join our global team as an Associate Director, Regulatory Affairs CMC. In this role, you will be responsible for leading the regulatory strategy and submissions for Kite's existing commercial and/or clinical programs within the EU region. You...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Job Summary:Gilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Regulatory Strategy. This role will be responsible for providing strategic guidance and oversight to our in-market partners in the Gilead Patient Solutions (GPS) region, ensuring compliance with regulatory...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Job Summary:Gilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Regulatory Strategy. This role will be responsible for providing strategic guidance and oversight to our in-market partners in the Gilead Patient Solutions (GPS) region, ensuring compliance with regulatory...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Job SummaryGilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs professional to join our global team as an Associate Director, Regulatory Affairs CMC. In this role, you will be responsible for defining the regulatory strategy, plans, and objectives for assigned products or projects.Key ResponsibilitiesAct as one of the EU...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full time

    Job SummaryGilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs professional to join our global team as an Associate Director, Regulatory Affairs CMC. In this role, you will be responsible for defining the regulatory strategy, plans, and objectives for assigned products or projects.Key ResponsibilitiesAct as one of the EU...


  • Cambridge, Cambridgeshire, United Kingdom Hyper Recruitment Solutions LTD Full time

    Job Title: Director of Business OperationsCompany: Hyper Recruitment Solutions LTDLocation: RemoteJob Type: Full-timeSalary: £110,000 - £130,000/annumBenefits: Flexible benefits and on-target bonus, hybridJob Description:Overview:We are seeking a highly experienced Director of Business Operations to join our team at Hyper Recruitment Solutions LTD. As a...


  • Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time

    Job DescriptionJob Title: Director, Global Regulatory Affairs, OncologyJob Summary:We are seeking a highly experienced and skilled Director, Global Regulatory Affairs, Oncology to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and executing regulatory strategies for our assigned programs and...


  • Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time

    Job DescriptionJob Title: Director, Global Regulatory Affairs, OncologyJob Summary:We are seeking a highly experienced and skilled Director, Global Regulatory Affairs, Oncology to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and executing regulatory strategies for our assigned programs and...