Senior Medical Writer, Medical Communications

About the role

This role offers the opportunity to work at the intersection of cutting-edge research and strategic storytelling, partnering with leading pharmaceutical and biotech clients.

Responsibilities

• Develop high-quality scientific content that supports strategic communication initiatives across a variety of therapeutic areas.
• Create content such as slide decks, executive summaries, and meeting materials, ensuring all deliverables are client-ready and scientifically rigorous.
• Collaborate closely with cross-functional teams, including medical, editorial, and client stakeholders, to shape clear and compelling narratives.
• Support the medical/legal/regulatory (MLR) review process by addressing feedback, incorporating revisions, and ensuring compliance with all guidelines.

Requirements

• 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

Qualifications

• Exceptionally curious, with strong domain knowledge across therapeutic areas, regulatory standards, and key statistical concepts
• An exceptional writer, able to translate complex data into clear, compelling, and accurate narratives
• Detail-oriented and committed to maintaining data integrity while tailoring content to specific audiences
• Highly organized and thrive in deadline-driven environments, taking ownership of quality and timelines
• A collaborative team player, skilled at partnering with clients, editors, and scientific leaders
• An analytical thinker who can interpret results, identify limitations, and communicate insights effectively

Skills

• Strong writing and communication skills
• Ability to manage multiple projects simultaneously
• Knowledge of scientific and regulatory standards
• Proficiency with relevant software tools

Benefits

Details not specified.

Pay

$95,000 - $125,000 USD

Schedule

Details not specified.