Bicara Therapeutics

Bicara Therapeutics

Associate Director, Global Scientific Communications

Boston · Director

Sponsorship not specifiedDetected 16 days ago
ComplianceVendor ManagementScientific WritingResearchAnimal StudiesLeadershipCommunicationCollaborationPublic Speaking

About the role

  • This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week.
  • Bicara Therapeutics is a clinical-stage biotech company pioneering bifunctional antibodies for targeted tumor modulation.
  • For more information, please visit www.bicara.com http://www.bicara.com.

Responsibilities

  • Cross-Functional Leadership: Lead the Publications Planning Team to drive development of the global publication plan, incorporating strategic input from Clinical Development, Research, Biostats, Regulatory, Legal, and Corporate Communications.
  • Lead the Publications Planning Team to drive development of the global publication plan, incorporating strategic input from Clinical Development, Research, Biostats, Regulatory, Legal, and Corporate Communications.

Requirements

  • Organizational Excellence: Exceptional organizational and time-management skills, with a proven ability to prioritize a high volume of deliverables in a fast-paced, deadline-driven environment.
  • Exceptional organizational and time-management skills, with a proven ability to prioritize a high volume of deliverables in a fast-paced, deadline-driven environment.
  • Education: Advanced degree (PhD, PharmD, MD, or MSc) with 6+ years of experience in Medical Affairs, Scientific Communications, or Publication Management.
  • Compliance & Guidelines: Expert knowledge and practical application of Good Publication Practices (GPP2022) and ICMJE guidelines.
  • Data Interpretation & Communication: Strong ability to interpret clinical trial data and simplify complex scientific concepts into clear, accurate medical messaging.
  • Project & Vendor Management: Strong hands-on experience managing external medical writing and scientific communication agencies, ensuring strict timeline adherence and budget management.
  • Cross-Functional Collaboration: Proven ability to influence and manage stakeholder input across a highly matrixed cross-functional team (e.g., Clinical, Biostats, Regulatory, Legal).
  • Attention to Detail: Meticulous editorial and review capabilities with strong compliance awareness and dedication to quality control.
  • Professional Certification: ISMPP Certified Medical Publication Professional (CMPP) credential is highly desirable.
  • System Familiarity: Proficiency with modern publication management software (e.g., iEnvision/Datavision, PubsHub) and Medical-Legal-Regulatory (MLR) review platforms (e.g., Veeva PromoMats/MedComms).
  • Scientific Writing: Strong scientific writing background, capable of providing rigorous directional feedback to agency partners.

Nice to have

  • Oncology or immuno-oncology experience is highly preferred.
  • Therapeutic Area Expertise: Oncology or immuno-oncology experience is highly preferred.

Benefits

  • Review & Compliance: Facilitate author and internal reviews, including navigating the Medical-Legal-Regulatory (MLR) approval process, while ensuring strict compliance with GPP2022 and ICMJE guidelines.
  • Vendor & Budget Oversight: Partner with and manage external scientific communication and medical writing agencies to ensure high-quality deliverables, timeline adherence, and budget optimization.
  • Scientific Messaging Alignment: Ensure all generated publications and medical deliverables strictly align with the established SCP, core lexicon, and broader Medical Affairs strategy set by leadership.
  • Operational Integration: Partner with internal teams to pull the established scientific narratives through into ongoing Medical Affairs activities, maintaining message consistency across global and regional outputs.
  • SCIENTIFIC CONTENT DEVELOPMENT (MSL & FIELD MEDICAL SUPPORT) (20%)
  • Field Resource Creation: Assist with development of high-impact medical slide decks, FAQs, training materials, and interactive educational tools to enable effective field-based scientific exchange.
  • Congress & Advisory Support: Support preparation of data-driven materials for medical advisory boards and key scientific congresses.
  • Data Continuity: Partner with Clinical Development and Medical Strategy to ensure incorporation of new clinical data into field-facing materials.
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