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Chief Scientific Officer

Roles & Responsibilities

  • PhD, MD, or equivalent in radiochemistry, nuclear medicine, oncology, pharmacology, or related discipline with significant radiopharmaceutical or oncology drug development experience.
  • Recognized expertise in radioligand therapy and radiopharmaceutical development with a strong scientific publication record.
  • Experience leading teams or programs within a CRO, biotech, or pharmaceutical company and supporting IND-enabling programs for radiopharmaceuticals.
  • Established global network within radiopharmaceutical and oncology communities with the ability to engage biotech/pharma sponsors and regulators.

Requirements:

  • Represent the company as a key opinion leader (KOL) in the global radiopharmaceutical and oncology community; present scientific data at major conferences and sponsor meetings; build relationships with biotech/pharma leaders and academic institutions.
  • Provide scientific guidance to sponsors across discovery, preclinical development, and IND-enabling stages; participate in strategic scientific discussions to accelerate decision-making and regulatory readiness; partner with commercial and operations teams to ensure scientific excellence in sponsor programs.
  • Guide the development of new scientific capabilities aligned with evolving radiopharmaceutical needs; identify opportunities in radiochemistry, biodistribution and dosimetry, imaging, translational tumor models, and IND-enabling study design; foster innovation through mentorship.
  • Serve as a scientific advisor to internal teams; mentor scientists and contribute to the development of future leaders; oversee direct and matrix management and operating budgets as assigned by the CEO; supervise PhD students and postdoctoral fellows through collaborations with academic centers.

Job description

What can we offer you?

Apart from job satisfaction, we can offer you:

HEALTH

  • Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA)

YOURSELF

  • Paid time off policy including holidays and sick time

  • Internal growth and development programs & trainings

WEALTH

  • 401(k) program, life & accident insurance and disability insurance

Key Responsibilities

External Scientific Leadership

  • Serve as a key opinion leader (KOL) representing the company within the global radiopharmaceutical and oncology research community.
  • Present scientific data and thought leadership at major industry conferences, scientific symposia, and sponsor meetings.
  • Lead seminars, webinars, and workshops that educate sponsors and the broader field on best practices in RLT development.
  • Build relationships with biotech/pharma leaders, academic institutions, and industry collaborators.

Sponsor Engagement & Scientific Partnership

  • Provide scientific guidance to sponsors developing radioligand therapies across discovery, preclinical development, and IND-enabling stages.
  • Participate in strategic scientific discussions with clients to design studies that accelerate decision-making and regulatory readiness.
  • Partner with the commercial and operations teams to ensure scientific excellence in sponsor programs.

Capability Development

  • Guide the development of new scientific capabilities aligned with the evolving needs of radiopharmaceutical developers.
  • Identify opportunities to expand the company’s expertise in radiochemistry, biodistribution and dosimetry, imaging, translational tumor models, and IND-enabling study design
  • Foster innovation across the organization through scientific mentorship and collaboration.

Scientific Excellence & Internal Leadership

  • Serve as a scientific advisor to internal teams, ensuring rigor, innovation, and quality across all studies.
  • Mentor scientists and contribute to the development of the next generation of leaders in radiopharmaceutical research.
  • Promote a culture of scientific curiosity, collaboration, and excellence.
  • Direct management responsibilities, including (but not necessarily limited to):
  • Line management
  • Matrix management of projects across internal and external interfaces.
  • Responsibility for such operating budgets as is assigned by the CEO
  • Supervision of PhD students/Postdoctoral fellows through on-going relationships with leading academic or other centres will be encouraged.

Key Success Metrics

  • Expansion of the company’s scientific reputation and visibility within the radiopharmaceutical field.
  • Development of new capabilities aligned with sponsor demand.
  • Increased strategic engagement with biotech and pharmaceutical partners.
  • Contribution to the successful advancement of sponsor programs toward IND and clinical development.

Experience, Education, and Certifications

  • PhD, MD, or equivalent advanced degree in radiochemistry, nuclear medicine, oncology, pharmacology, or related discipline.
  • Significant experience in radiopharmaceutical or oncology drug development.
  • Recognized expertise in radioligand therapy and radiopharmaceutical development.
  • Strong scientific publication record and experience presenting at major scientific conferences.
  • Experience working with biotech/pharma sponsors in preclinical or translational research
  • Prior leadership experience within a CRO, biotech, or pharmaceutical company.
  • Experience supporting IND-enabling programs for radiopharmaceuticals.
  • Familiarity with regulatory expectations for radiopharmaceutical development.
  • Established network within the radiopharmaceutical and oncology communities.
  • Proven ability in managing complex scientific projects in a multi-disciplinary environment.
  • Proven experience in networking with academia and industry.
  • Viewed as a key opinion leader internationally in the field of imaging.

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