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Director, Global Medical Communications

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

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