Head of Corporate Affairs and Public Affairs

2 weeks ago


San Diego, United States RayzeBio Full time

Job Title: Head of Corporate Affairs and Public Affairs

Location: San Diego


Background

RayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio operates as a standalone entity within the BMS organization, maintaining its biotech culture with the opportunity to leverage the best-in-class oncology capabilities of BMS. RayzeBio is developing innovative drugs against targets of solid tumors. The lead asset, RYZ101, is in Phase 3 testing for patients with gastroenteropancreatic neuroendocrine tumors (GEP-NETs), as well as earlier stage testing for patients with small cell lung cancer (SCLC). Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.


Summary

The Head of Corporate Affairs and Public Affairs is a key member of an entrepreneurial leadership team with a shared vision to build the leading radiopharmaceutical company. The ideal candidate will possess a deep knowledge of communications, specifically with a proven ability to successfully strategize and deploy corporate and asset-level messaging for clinical to commercial stage oncology biotechnology companies. The role needs an accomplished and confident leader with hands-on experience creating, executing and measuring creative and impactful communications campaigns to position the company ahead of upcoming development milestones. The candidate should have experience navigating and engaging a diverse group of stakeholders to support RayzeBio and RPT advancement for the benefit of patients.

The role is expected to serve as a liaison between the Bristol Myers Squibb Corporate Affairs, Investor Relations, and Issues Advocacy teams and RayzeBio. It requires the ability to navigate between the culture of small biotech while integrating with a broader corporate structure. Optimal candidates should have experience working both in small biotech as well as within larger corporate structures.

The ideal candidate will be results-oriented and directly responsible for helping to foster a culture that emphasizes cooperation, teamwork and respect.


Job Responsibilities

Essential duties and responsibilities include the following. Other duties may be assigned.

  • Provide strategic and operational leadership for RayzeBio Corporate Affairs, including internal communications, external communications, and executive thought leadership.
  • Develop and deploy comprehensive corporate and asset communication campaigns to successfully advance RayzeBio and Bristol Myers Squibb corporate positioning.
  • Utilize a deep understanding of corporate communications principles to identify and execute in areas of opportunity for engagement, education, and advancement of RayzeBio strategic priorities.
  • Possess strong media relationships, build, and grow the RayzeBio presence externally and serve as spokesperson to represent RayzeBio.
  • Understand and navigate issues related to RPT advancement for the benefit of patients. Partner closely with Bristol Myers Squibb government affairs teams to advance policies in support of patients.
  • Build and grow knowledge of RayzeBio differentiators with stakeholders, including KOLs, patient advocates, patients, and caregivers to advance knowledge of RPT technology.
  • Work as the executive communicator for members of the RayzeBio leadership team, including the President and other members, creating tailored messaging tracks, developing, and supporting executive visibility campaigns.
  • Operate as a liaison between Bristol Myers Squibb Corporate Affairs and Investor Relations teams to ensure messaging continuity, engagement, and corporate alignment.
  • Advise RayzeBio leadership and Bristol Myers Squibb leaders on key strategic communications to uphold a positive image and reputation for the organization.
  • Develop and build an internal culture of cooperation, teamwork, and respect through internal communications initiatives. Establish an internal communications framework to support the needs of RayzeBio.
  • Create and manage department and project budgets, internal, external resources in support of corporate goals.

Education and Experience

  • Masters degree in communications, journalism or similar field.
  • 15 + years of leadership experience in pharmaceutical/biotech corporate affairs environments.
  • Demonstrated ability to build and lead high functioning cross-functional corporate teams and a record of getting things done in small biotech settings. Demonstrated ability to navigate relationship with large parent company.
  • Experience building and leading lean, effective departments.
  • Understanding of oncology drug development, advancement, and commercialization. Demonstrated ability to articulate and differentiate complex scientific topics to a diverse range of stakeholders.
  • Demonstrated ability to engage a diversity of stakeholders across issues and forming trusted relationships.
  • Experience counseling, developing, and supporting C-suite and leadership thought leadership.
  • Crisis communications experience in the biotechnology and/or pharma sectors.
  • Deep knowledge and relationships with priority media. Experience serving as corporate spokesperson.

Skills and Qualifications

  • Excellent written and oral communication skills and ability to work in a fast-paced, dynamic, and collaborative environment.
  • High EQ, Strong interpersonal, organizational and communication skills and ability to motivate and drive productivity in small company environments.
  • Ability to effectively partner cross-functionally to achieve results.
  • Ability to successfully establish and manage relationships including PAGs, KOLs, patients, caregivers, and industry partners.
  • Experience building relationships with media, government, and other external bodies.
  • Ability to translate strategy / complex material into clear communication plans and messaging.
  • Emergency media response experience and confidence in handling media enquiries in a crisis.
  • Ability to prioritize, work under pressure and deliver to deadlines.



  • San Antonio, United States U.S. Army Medical Command Full time

    Summary About the Position: Serves as a Social Media Manager and a Public Affairs Specialist for OTSG/MEDCOM. Conducts the public affairs program for the . Army Medical Command (MEDCOM), with responsibility for planning, developing and communicating the organization's programs, policies and activities to the stakeholders, beneficiaries and the...


  • San Francisco, United States ALSTOM Full time

    Leading societies to a low carbon future, Alstom develops and markets mobility solutions that provide the sustainable foundations for the future of transportation. Our product portfolio ranges from high-speed trains, metros, monorail, and trams to integrated systems, customised services, infrastructure, signalling and digital mobility solutions. Joining us...


  • San Francisco, United States Alstom Full time

    Leading societies to a low carbon future, Alstom develops and markets mobility solutions that provide the sustainable foundations for the future of transportation. Our product portfolio ranges from high-speed trains, metros, monorail, and trams to integrated systems, customised services, infrastructure, signalling and digital mobility solutions. Joining us...


  • San Diego, United States Device Search Group Defunct Full time

    We are seeking an experienced Senior Director or Vice President of Regulatory Affairs (DOE). As the head of Regulatory Affairs you will be responsible for leading and managing all aspects of Clinical and CMC Regulatory Affairs. The ideal candidate will have a strong background in cell therapy with experience in early development regulatory affairs (pre-IND...


  • San Diego, United States Device Search Group Full time

    We are seeking an experienced Senior Director or Vice President of Regulatory Affairs (DOE). As the head of Regulatory Affairs you will be responsible for leading and managing all aspects of Clinical and CMC Regulatory Affairs. The ideal candidate will have a strong background in cell therapy with experience in early development regulatory affairs (pre-IND...


  • San Diego, United States Device Search Group Full time

    We are seeking an experienced Senior Director or Vice President of Regulatory Affairs (DOE). As the head of Regulatory Affairs you will be responsible for leading and managing all aspects of Clinical and CMC Regulatory Affairs. The ideal candidate will have a strong background in cell therapy with experience in early development regulatory affairs (pre-IND...


  • San Francisco, California, United States City and County of San Francisco Full time

    Job Description The 5642 Senior Policy and Public Affairs Coordinator serves as the operational hub for legislative and Commission activities at the Department. The position sits at the nexus between the Mayor’s Office, the Commission, the Board of Supervisors, other City agencies, and the Department’s Program Managers. Reporting to the Chief Policy and...


  • San Diego, United States Aequor Technologies Full time

    US Regulatory Affairs Lead ------------------------------------------------------------------------------------------------- SCOPE OF RESPONSIBILITIES: " He/She will be responsible for representing regulatory function to approve promotional material " He/She will be at ease working in a matrix environment and be able to navigate ambiguity to drive decision...


  • San Diego County, United States County of San Diego California Full time

    The Office of Chairwoman Nora Vargas is recruiting an experienced and outstanding professional to serve as Chief of Intergovernmental Affairs for District 1. Under the leadership of Chairwoman Vargas, and reporting to the Chief of Staff, the Chief of Government, Chief, Assistant, Relationship, Public Relations, Policy, Business Services


  • San Diego, United States Genalyte Full time

    Here at Genalyte, you will find yourself working with talented individuals inspired by our vision, eager to make an impact on the patient experience, and who share a common goal of getting our technology into every physician’s office. We have a great opportunity for a Regulatory Affairs Specialist to join our team! **ABOUT THE ROLE** The Regulatory...


  • San Diego, United States Cypress Human Capital Management, LLC Full time

    Regulatory Affairs Specialist The Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. They will also coordinate clinical study trials, including offsite location for trials when needed. Essential...


  • San Francisco, California, United States Department Of Veterans Affairs Full time

    Summary Employee will serve as a Visual Information Specialist located at the Veterans Affairs Health Care System in San Francisco, CA. Duties ***THIS IS NOT A VIRTUAL POSITION, YOU MUST LIVE WITHIN OR BE WILLING TO RELOCATE WITHIN A COMMUTABLE DISTANCE OF THE DUTY LOCATION***This position involves a multi-grade career ladder. The major duties listed below...


  • South San Francisco, United States Maze Therapeutics Full time

    The Position: Join our dynamic Regulatory Affairs team as a Director, Regulatory Affairs, where you will be the driving force behind our development programs from preclinical candidate designation through drug approval. We are looking for a strategic thinker and regulatory expert to provide leadership and guidance. As the Global Program Lead, you will...


  • San Francisco, United States Bechtel Full time

    Requisition ID:  269631 Relocation Authorized:  Limited (e.g. Development Assignment) Telework Type: Full-Time Office/Project  Work Location: Richland, WA  Hourly Range: $20.05/hour - $27.60/hour (Determined by function, education, experience, and qualifications of the applicant. A 15% salary uplift is provided on top of base salary for...


  • San Diego, United States Cypress HCM Full time

    Regulatory Affairs Specialist The Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. They will also coordinate clinical study trials, including offsite location for trials when needed. Essential...


  • San Antonio, United States Extremity Care Full time

    Job DescriptionJob DescriptionSalary: $90KPurpose:The Regulatory Affairs Manager is responsible for managing the regulatory affairs department and functions to ensure regulatory compliance of quality management system.Duties & Responsibilities: Review and approve audit agenda, plan, summary reports for internal audits. Facilitate and participate in external...


  • San Antonio, United States Extremity Care Full time

    Job DescriptionJob DescriptionSalary: $90KPurpose:The Regulatory Affairs Manager is responsible for managing the regulatory affairs department and functions to ensure regulatory compliance of quality management system.Duties & Responsibilities: Review and approve audit agenda, plan, summary reports for internal audits. Facilitate and participate in external...


  • San Diego, United States Cypress HCM Full time

    Regulatory Affairs SpecialistThe Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. They will also coordinate clinical study trials, including offsite location for trials when needed. Essential...


  • San Diego, United States Cypress HCM Full time

    Regulatory Affairs SpecialistThe Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. They will also coordinate clinical study trials, including offsite location for trials when needed. Essential...


  • South San Francisco, United States Maze Therapeutics Full time

    Job DescriptionJob DescriptionThe Position:Join our dynamic Regulatory Affairs team as a Director, Regulatory Affairs, where you will be the driving force behind our development programs from preclinical candidate designation through drug approval. We are looking for a strategic thinker and regulatory expert to provide leadership and guidance. As the Global...