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Artiva Biotherapeutics

Senior Director/Executive Director, Medical Affairs, Medical Communications, Publications

Artiva Biotherapeutics

Sr. Director/Executive Director of Medical Communications for biotech company focused on NK cell-based therapies.

Posted 6/25/2026full-timeRemote • California • 🇺🇸 United StatesSenior💰 $250,000 - $300,000 per yearWebsite

About the role

Key responsibilities & impact
  • Drive the end-to-end strategic planning and execution of scientific publications across the AlloNK platform
  • Develop and execute global/regional publication plans (abstracts, posters, manuscripts, reviews) for rheumatology, immunology, and cell therapy audiences
  • Collaborate with Clinical Development, Medical Affairs, and principal investigators to ensure timely, accurate dissemination of clinical trial results at major scientific congresses
  • Ensure all publications strictly adhere to Good Publication Practice (GPP), ICMJE authorship guidelines, and corporate compliance standards
  • Oversee the drafting, editing, and medical review of scientific publications and related congress materials, ensuring scientific accuracy and balanced data presentation
  • Direct external medical communications agencies, medical writers, and vendor budgets to ensure on-time, high-quality deliverables
  • Architect the comprehensive pre- and post-congress communication strategy for major rheumatology and immunology meetings (e.g., ACR, EULAR, ISSJD, CCR) including congress playbooks and post-congress debriefs
  • Lead the development of congress-specific materials, including scientific symposia, medical booth content, and interactive learning stations
  • Monitor emerging clinical data, treatment paradigm shifts, and competitor activity at key meetings, translating these external insights into actionable communication strategies

Requirements

What you’ll need
  • Advanced scientific or clinical degree (e.g., PhD, PharmD, DO, or MD) required
  • 8+ years of progressive medical communications or publications experience within the biotech or pharmaceutical industry
  • Proven track record and deep understanding of rheumatology, immunology, and/or complex cell therapies (e.g., CAR-T, TCEs)
  • Expert knowledge of ICMJE guidelines, GPP guidelines, and the Sunshine Act/EFPIA disclosure requirements
  • Demonstrated ability to lead cross-functional teams, build a medical communications and publications capability, manage and mentor junior staff, and manage multiple complex projects simultaneously.
  • Experience utilizing publication management software (e.g., Datavision) to track publication progress and manage author review cycles
  • Strong network of relationships with Key Opinion Leaders (KOLs) in rheumatology, immunology, and cell therapy
  • Exceptional scientific storytelling ability and meticulous attention to detail
  • ISMPP CMPP certification

Benefits

Comp & perks
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Recognition program with Bonus.ly

ATS Keywords

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Hard Skills & Tools
scientific publicationspublication planningmedical writingclinical trial results disseminationdata presentationcommunication strategyproject managementscientific storytellingrheumatologyimmunology
Soft Skills
leadershipcollaborationmentoringattention to detailnetworkingcross-functional team managementstrategic planningexecutioncommunicationproblem-solving
Certifications
ISMPP CMPP certification