Director – Medical Communications

Role Overview

• Publish Operations & Congress Execution: Lead the Global Publication Planning Team cadence (agendas, decisions, timelines, action tracking) and execute the rolling 12-24 month publication plan.
• Drive end-to-end delivery of peer-reviewed and congress outputs (abstracts, manuscripts, posters, oral presentations), including author coordination and internal review cycles.
• Launch & Market Preparation Evidence Dissemination: Execute high-priority anzu-cel market preparation tactics, including manuscripts and congress packages that support clinical practice adoption, competitive differentiation, and launch readiness.
• Scientific Platform & Lexicon: Develop, maintain, and operationalize the Scientific Platform & Lexicon for anzu-cel and priority programs (core scientific narrative, terminology standards, claims language).
• Insight Generation & Scientific Exchange: Operationalize an “insight engine” across advisory boards, publication data review meetings, and congress debriefs.
• Vendor & Team Leadership: Lead day-to-day Medical Communications vendor execution: scopes of work, resourcing plans, quality standards, timelines, and performance scorecards/quarterly business reviews.

Requirements

• Advanced scientific/medical degree required (MD, PharmD, PhD, or APN)
• 10 years of experience in Medical Communications/Publications within biotech/pharma and/or agency environments, including demonstrated leadership of global publication plans and major congress execution
• Demonstrated success leading cross-functional scientific narrative development and operating in a fast-paced, milestone-driven environment (e.g., launch readiness, major data disclosures)
• Demonstrated ability to build and govern a Scientific Platform/Lexicon that drives consistent global dissemination across publications, congresses, and scientific exchange
• Experience supporting Medical Affairs and Commercial teams from pre-launch through launch , with demonstrated ability to adapt content needs across product lifecycle stages
• Strong expertise in publication operations, scientific writing, data interpretation, and compliant review processes
• Demonstrated prior experience with insight generation , including design and execution support for advisory boards, KOL engagement activities, publication/data review meetings, congress debriefs, and synthesis of insights into actionable recommendations
• Demonstrated prior training experience , including developing and delivering scientific training content for Medical Affairs and/or cross-functional stakeholders (e.g., launch readiness, Scientific Platform/Lexicon training, publication processes, congress readiness)
• Vendor management experience (scope, quality, timelines, budget, performance)

Benefits

• Competitive rates for Health, Dental, and Vision Insurance
• 4 weeks of Paid Time off, granted up front each year and prorated for first and last year of employment.
• Sick Time Off – 56 hours
• 12 Paid Holidays
• 100% Employer-Paid Life Insurance up to at 1x annual salary, up to one hundred thousand ( club together)
• 100% Employer Paid Short
• and Long-Term Disability Coverage
• 401(k) with Immediate Eligibility & company match
• Partially paid Parental Leave for eligible employees. (3 weeks)
• Additional voluntary employee paid coverages including Accident, Hospital Indemnity, and Critical Illness
• Employee Paid Identity Theft Protection and Pet Insurance.
• Opportunities to work with leading experts in the field of T-cell immunotherapy.
• Company provided learning and development opportunities
• Fast paced, high demand collaborative and dynamic environment.