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Biotechnology, Pharmaceuticals

Senior Manager / Associate Director, Publications and Medical Information (Contract)

Brisbane, CAOnsiteContractDirectorPosted 1 month agoVisa sponsorship available

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Required skills

  • Publications
  • Medical Information
  • GPP
  • ICMJE
  • MLR
  • Standard Response Letters
  • Scientific Writing
  • Project Management

Nice to have

  • AI
  • Data Review
  • Congress Support
  • KOLs

Role summary

Nurix Therapeutics, a clinical-stage biopharmaceutical company specializing in targeted protein degradation medicines for cancer and inflammatory diseases, seeks a Sr. Manager / Associate Director for Publications and Medical Information on a contract basis. This role involves contributing to and executing publication strategies, managing the drafting and review process for clinical publications, and supporting data review slide decks. The position also requires providing Medical Information support at congresses, drafting Standard Response Letters, ensuring timely responses to medical inquiries, and creating FAQs. The ideal candidate will have a doctoral degree and 3-5 years of experience in Medical Affairs, Communications, Publications, or Information, with strong knowledge of GPP, ICMJE, and MLR processes, excellent scientific writing, project management, and collaboration skills.

Senior Manager / Associate Director, Publications and Medical Information (Contract)

Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.

Job Responsitities:

Publications

  • Contribute to development of Publication Strategy and Publication Plan (in coordination with the Publications Working Team)
  • Execute publication tactics and the Publication Plan
  • Manage the drafting process for clinical publications (with vendor/agency), tracking timelines and ensuring timely reviews, approvals, and submissions
  • Interact with internal and external authors/KOLs related to clinical publications
  • Manage record keeping and digital storage for publications-related materials, including publications metrics

    • Data Reviews

  • Contribute to development of data review slide decks and derivative materials (with vendor/agency)
  • Support data presentation-related AI projects

    • Congress Support

  • Support booth staffing, congress materials, and presentation logistics (in coordination with Medical Affairs Operations)
  • Provide dedicated congress/booth Medical Information support

    • Medical Information

  • Draft Standard Response Letters and manage related Medical and Legal review
  • Ensure timely responses to medical inquiries; coordinate with the Medical Information team at a partner company and track inquiry volumes
  • Create FAQs and reference materials (in coordination with internal Subject Matter Experts)
  • Support Medical Information-related AI projects

    • Education:

  • Doctoral degree in a medical, biological, or related discipline (PhD, PharmD, MD; MS with relevant experience considered)

    • Experience:

  • 3-4 years of experience (Sr. Manager) or 4-5 years of experience (Associate Director) in Medical Affairs, Medical Communications, Clinical Publications, or Medical Information
  • Demonstrated experience managing scientific/clinical publications end-to-end
  • Familiarity with publication management and MLR processes/procedures
  • Experience with medical information operations and Standard Response Letter (SRL) development

    • Skills:

  • Strong working knowledge of GPP, ICMJE, and industry compliance requirements
  • Excellent scientific writing, editing, and critical literature-review skills
  • Excellent communication skills
  • Project management and time management skills, with the ability to operate within multiple concurrent timelines
  • Cross-functional collaboration skills, with the ability to align with internal teams of Subject Matter Experts representing different functions

    • Fit with Nurix Culture and Values

  • Strong team orientation; highly collaborative
  • Solutions and results-oriented focus
  • Hands-on approach; resourceful and open to diverse points of view

    • Location: Brisbane, CA - Onsite

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