Join Immatics and shape the future of cancer immunotherapy; one patient at a time!
Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.
Why Join Us?
We are seeking a Director, Medical Communications to support our Medical Affairs team. This role will lead global medical publications, congress strategy, and launch-critical scientific dissemination for Immatics' priority programs, with a focus on anzu-cel market preparation and launch readiness.
The Director is responsible for the high-quality, compliant delivery of manuscripts, abstracts, and scientific materials that translate emerging data into clear, decision-enabling narratives for internal and external stakeholders, informed by insights from advisory boards, publication reviews, and congress activities.
Additionally, this role will own the Scientific Platform & Lexicon for anzu-cel and key programs, and drive a scalable data dissemination engine (in partnership with internal teams and agencies) to ensure consistent output, strategic data cadence, and measurable scientific impact and share of voice.
FLSA Classification: Salary, Exempt
Schedule: 8:00 AM - 5:00 PM; Monday to Friday
Reports to: Senior Director, Medical Communications
Location: Fully Remote
Salary: $220,000 - $270,000
What You'll Do:
As a Director, Medical Communications, you will play a key role in supporting our Medical Affairsoperations:
Publication Operations & Congress Execution
Lead theGlobal Publication Planning Teamcadence (agendas, decisions, timelines, action tracking) and execute the rolling 12-24 monthpublication plan.
Drive end-to-end delivery of peer-reviewed and congress outputs (abstracts, manuscripts, posters, oral presentations), including author coordination and internal review cycles.
Own author/KOL strategy for priority publications (target journals/congress slots, authorship planning, competitive differentiation, and submission positioning)
Leadcongress strategy and readinessfor priority meetings (e.g., ASCO/ESMO/SITC/SMR/SGO), including narrative strategy, data packages, internal review governance, and post-congress dissemination planning
Launch & Market Preparation Evidence Dissemination
Execute high-priorityanzu-cel market preparationtactics, including manuscripts and congress packages that supportclinical practice adoption, competitive differentiation,and launch readiness
Lead publication tactics involvingcomplex analyses(secondary/tertiary/post hoc exploratory) and/ornontraditional datasets(e.g., compassionate use case studies, collaborative translational analyses with academia, and patient-authored manuscripts whereappropriate)
Partner with cross-functional teams to translate evidence intomedical education and scientific enablementneeds (e.g., narrative modules, FAQs, scientific decks) that stand up to peer review and KOL scrutiny,maintainclear separation from promotional content, and adhere to compliance guardrails
Develop,maintain, and operationalize theScientific Platform & Lexiconforanzu-cel and priority programs (core scientific narrative, terminology
standards, claims language, data interpretation guardrails, data tables, and approved phrasing)
Ensure consistent scientific language and message discipline across publications, congress assets, advisory board materials, and insight outputs
Drive platform adoption by ensuring it is embedded intopublication briefs, congress plans, advisory board materials, medical training, and insight frameworks
Insight Generation & Scientific Exchange
Capture, synthesize, and communicate insights (themes, risks, opportunities) back to Medical Affairs and cross-functional stakeholders to inform strategy and evidence planning
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
Own agency governance, budget stewardship, and performance scorecards; drive continuous improvement in cycle time, quality, and stakeholder satisfaction
Build scalable processes (templates, checklists, SOPs) that improve quality, compliance, and cycle time
Training & Development
Compliance & Quality
Ensure all scientific communications adhere to applicable publication ethics and company standards (e.g., ICMJE/GPP) including authorship, COI, transparency (data-sharing, traceable review history), andappropriate documentation.
Required Experience and Education:
Demonstrated success leadingcross-functional scientific narrative developmentandoperatingin a fast-paced, milestone-driven environment (e.g., launch readiness, major data disclosures)
Strongexpertisein publication operations, scientific writing, data interpretation, and compliant review processes
Demonstrated prior experience withinsight 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 priortraining 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)
Preferred Experience and Education:
Background with TCR T-cell therapies, CAR T-cell therapies, or other adoptive cell therapies, including experience in developing scientific communication strategy and tactics such as peer-reviewed publications
Experience working with complex analyses and/or nontraditional datasets (e.g., compassionate use, external collaborations, translational packages)
Demonstrated prior experiencesupporting launch and market access evidence needs, including prior success withone or more of the following: submissions toNCCN,CMS NTAP, and/orICER; development ofAMCP and/or Global Value Dossier (GVD).
Competencies:
Work Environment:
This position is remote and should be performed in an office setting that simulates the work office environment. This office must be set up in a way that allows for privacy and quiet during work hours, as well as a comfortable chair and desk. This position uses phone, computer, office equipment and supplies on a regular basis. Noise levels should be at a level which would allow for proper communication with other members virtually.
Travel required: Up to 25% to congresses, advisory boards, and key internal meetings
Physical demands:
Hearing - the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds.
Work authorization/security clearance requirements:
Legal eligibility to work in the United States is required. Immatics participates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment.
Affirmative Action/EEO statement:
Immatics is an equal opportunity employer. All employment decisions including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs.We do not discriminate on the basis of race, color, religion, national origin, ethnicity, marital status, age, physical or mental disability, medical conditions, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
What do we offer?
At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics
Comprehensive Benefits:
The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.