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Director, Global Medical Communications

Bicara Therapeutics
Full-time
Remote friendly (Boston, MA)
United States
Medical Affairs

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Role Summary

Director, Global Medical Communications responsible for leading publication strategies and execution for assigned oncology assets. Reports to the Senior Vice President, Clinical & Medical Affairs. Based in Boston with a hybrid schedule (three in-office days per week). This role is ideal for a scientifically adept communicator who thrives under tight timelines, drives complex cross-functional projects, and translates clinical data into compelling scientific narratives, shaping external communication of Bicara’s science and building relationships with KOLs.

Responsibilities

  • Lead global publication strategy and tactical execution for assigned oncology assets, including manuscripts, abstracts, posters, oral presentations, CME initiatives, and other external scientific communications.
  • Define and evolve the scientific narrative and key messaging in collaboration with Clinical Development, Medical Affairs, and senior leadership, ensuring consistency across all communications.
  • Serve as the publications lead on cross-functional teams, including regular meetings with Clinical, Regulatory, Commercial, and medical colleagues; ensure alignment with scientific platforms, lexicons, gap assessments, and Medical Affairs plans.
  • Establish and operationalize scalable publication processes, including authorship alignment, internal review workflows (e.g., MLR), and submission protocols, in compliance with ICMJE, GPP, and internal publication policies.
  • Create and maintain a detailed publication plan and timeline, tracking status, prioritizing high-impact deliverables, and managing version control and publication records using internal tools.
  • Drive scientific content with strategic direction and provide initial input, partnering cross-functionally to ensure clarity, accuracy, and compliance.
  • Provide direction and oversight to external vendors and internal medical writers, ensuring deliverables are scientifically rigorous, timely, and on-budget.
  • Partner with the Clinical Development and Finance teams to forecast outsourcing needs, manage publication budgets, and optimize internal resource allocation for assigned assets.
  • Identify and address publication-related issues, providing timely solutions or mediation where needed, and ensuring alignment with cross-functional strategies.
  • Collaborate with Medical Affairs leadership to develop MSL materials, scientific slide decks, congress compendia, FAQs, and other medical communication tools.
  • Engage directly with KOLs and investigators to align on content development, data interpretation, authorship expectations, and congress strategy.
  • Ensure accurate documentation of publication activities, in compliance with company policy and global best practices (ICMJE, GPP, etc.).

Qualifications

  • Minimum 5 years’ experience in medical publications in a biotech or pharmaceutical setting; experience in small/mid-sized biotech is strongly preferred
  • Deep understanding of oncology, immuno-oncology, or related therapeutic areas; experience publishing clinical trial data
  • Proven track record of leading publications and medical communications across pre-launch and launch-stage assets
  • Excellent writing and editing skills with the ability to translate complex data into clear, accessible, and engaging content
  • Demonstrated ability to engage with KOLs, investigators, and authors to shape content and guide authorship strategy
  • Experience managing both external publication vendors and internal writers, with strong project and budget management capabilities
  • Solid understanding of industry guidelines and regulations, including ICMJE, GPP, and company publication policy
  • Comfortable using tools for project tracking, publication planning, and document management
  • Strong interpersonal, collaboration, and leadership skills across cross-functional teams and global stakeholders
  • Solution-oriented mindset: ability to foresee and resolve publication-related challenges proactively

Education

  • BS required; advanced scientific degree (PhD, PharmD, MD, or equivalent) preferred

Skills

  • Scientific writing and editing
  • Publication planning and project management
  • Cross-functional leadership and collaboration
  • KOL/investigator engagement and content development
  • Vendor and budget management
  • Knowledge of ICMJE, GPP, and internal publication policies