Sr. Manager, Scientific Communications

Key Responsibilities

• Develop and maintain scientific materials such as slide decks, flashcards/infographics, reactive and proactive field resources, social media posts, summaries, FAQs, training tools, standard/custom response letters and other medical communication assets.
• Support development of HEOR and value communication materials, including AMCP dossier sections, payer evidence decks, pre-approval information exchange resources materials, burden-of-illness summaries, and related access resources.
• Translate clinical, epidemiologic, and health economic evidence into concise, accurate, and audience-appropriate materials for internal and external stakeholders.
• Provide publication support through literature review, content drafting, data summarization, annotation support, poster or manuscript support materials, and congress pull-through activities as assigned.
• Cook up with cross-functional teams and external vendors to deliver high-quality materials on time and in alignment with scientific, medical, legal, and regulatory review requirements.

Skills & Attributes

• Strong scientific writing, editing, and content development skills with the ability to synthesize complex data into clear communications.
• Excellent attention to detail and commitment to scientific accuracy, reference integrity, consistency, and compliance.
• Proficiency with Microsoft Office and common review, annotation, and document-management systems and workflows (e.g. Veeva).
• Strong project management, prioritization, negotiation, and collaboration/stakeholder management skills in a fast-paced, biotech environment.
• Must have strong business acumen, ability to interface with matrix partners to make trade-off decisions.

Qualifications

• Advanced degree in a scientific, clinical, or healthcare-related discipline preferred (for example PharmD, PhD, MS, MPH, or equivalent).
• Approximately 1-3 years of relevant experience in pharmaceutical, biotechnology, medical communications, Medical Affairs, HEOR communications, or a related function.
• Experience supporting scientific content development such as slide decks, training resources, digital content, flashcards/infographics, evidence summaries, or payer-facing materials required.
• Experience in hypertension, cardio-renal disease, market access, HEOR, or product launch preparation is preferred.
• Strong understanding of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GPP, ICH, PhRMA Code).
• Able to manage vendors.