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Entrada Therapeutics · 3 weeks ago

Director, Scientific Communications

Boston, MA

Full-time

Hybrid

Director/Executive

$225K/yr - $253K/yr

8+ years exp

Entrada Therapeutics is a clinical-stage biopharmaceutical company focused on transforming patient lives through innovative medicines. The Director, Scientific Communications will lead the development and execution of the medical affairs publication and scientific communications strategy, ensuring scientific accuracy and collaboration across various teams.

BiotechnologyEmergency MedicineGeneticsHealth CareMedical

Responsibilities

Ensure the development and execution of publication, congress, training, scientific communication and medical education strategy across multiple platforms (conventional, digital, congress)

Conduct literature reviews and gap analyses to identify data needs, inform strategy, and guide development of scientific communication tactics

Ensure creation of high quality, scientifically accurate, and compliant deliverables including slide decks, disease state materials, manuscript summaries, program specific FAQs, congress summaries, advisory board materials, training materials and other internal and external resources

Develop program specific scientific materials such as mechanism of disease or action graphics, data summary decks, and templates for company wide use

Provide writing and editorial support for abstracts, posters, manuscripts, and other publications, including conducting literature searches and preparing annotated summaries for internal teams

Oversee congress activities including content development for Discovery/Research and Medical Affairs presence, abstract coverage, congress summaries, and all related deliverables in collaboration with Corporate Communications, Investor Relations, and Competitive Intelligence

Lead publication planning activities including cross functional coordination, management of review and approval processes for external and field based materials, tracking of company or investigator led publications, and ensuring adherence to publication and scientific exchange compliance requirements including GPP3, ICMJE, and Sunshine Act guidance

Provide project management support for Scientific Communications including maintenance of slide libraries and repositories, version control, process design and improvement, and implementation of innovative approaches such as digital tools and publication metrics tracking

Lead medical and scientific messaging for medical affairs and ensuring these messages are aligned across all forms of scientific, field and corporate messaging

Partner with and manage vendor(s) to lead the execution of the scientific communications plan overseeing medical writing agencies including project initiation, execution, and closing; working with authors on submissions to congresses, journals etc, managing revisions, and budget

Collaborate with cross-functional teams/colleagues to develop evidence generation, publication and congress activities to ensure insight sharing and alignment across teams, and efficient execution of strategies and tactics

Support market access efforts by developing appropriate medical materials and supportive documents and by providing medical expertise as required to internal and external stakeholders

Qualification

Medical Affairs ExperienceNeuromuscular Disease ExpertiseScientific Communication StrategyVendor ManagementProject ManagementCuriosityTenacityRegulatory UnderstandingCollaborationCreativity

Required

Must have an advanced medical degree (MD, DO, or equivalent), PharmD or PhD

8+ years of medical affairs experience in the Pharmaceutical/Biotechnology industry

Proven experience in working collaboratively and cross functionally across the enterprise field medical teams, corporate affairs clinical development, commercial, sales, market access and other key functions and demonstrated ability to inform and shape company/product strategy

Demonstrated understanding of laws, regulations, standards, and guidance governing the conduct of publications

Understanding of relevant GCP, ICH and FDA/EMA regulations

Ability to travel approximately 20% of the time both domestically and internationally, as determined by business needs