About the Job
Are you passionate about transforming complex science into meaningful, impactful communications that improve patient outcomes? This role offers the opportunity to work at the intersection of cutting-edge research and strategic storytelling, partnering with leading pharmaceutical and biotech clients. You’ll join a co...
Key Responsibilities
In this role, you will develop high-quality scientific content that supports strategic communication initiatives across a variety of therapeutic areas. You will be responsible for creating content such as slide decks, executive summaries, and meeting materials, ensuring all deliverables are client-ready and scientifically rigorous.
You’ll collaborate closely with cross-functional teams, including medical, editorial, and client stakeholders, to shape clear and compelling narratives. Additionally, you will support the medical/legal/regulatory (MLR) review process by addressing feedback, incorporating revisions, and ensuring compliance with all guidelines. Your work will directly contribute to delivering impactful solutions that help clients communicate science effectively and achieve their goals.
Required Skills & Abilities
You are scientifically curious, with strong domain knowledge across therapeutic areas, regulatory standards, and key statistical concepts
You are an exceptional writer, able to translate complex data into clear, compelling, and accurate narratives
You are detail-oriented and committed to maintaining data integrity while tailoring content to specific audiences
You are highly organized and thrive in deadline-driven environments, taking ownership of quality and timelines
You are a collaborative team player, skilled at partnering with clients, editors, and scientific leaders
You are an analytical thinker who can interpret results, identify limitations, and communicate insights effectively
Advanced scientific degree (PharmD, MD, or PhD)
2+ years of experience in a medical communications agency or similar environment
Strong experience developing scientific content across multiple formats (e.g., slide decks, publications, summaries)
Demonstrated ability to conduct comprehensive literature searches and synthesize findings
Proficiency with Microsoft Word®, PowerPoint®, Excel®, Adobe Acrobat®, and reference management tools (e.g., EndNote®)
Experience participating in or supporting MLR review processes
Experience working with Medical Affairs and/or Publications deliverables
Exposure to commercial content development
Familiarity with multiple therapeutic areas or complex disease states
Qualifications
Experience:
2 years experience
Education:
Postgraduate
