Senior Medical Writer, Medical Communications

Precision AQ
$95,000 - $125,000

About The Position

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 collaborative, high-performing team known for delivering best-in-class scientific communications and maintaining long-standing client relationships. If you’re energized by translating data into insights and thrive in a fast-paced, team-oriented environment, this is a standout opportunity to grow your career. 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.

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
  • Scientifically curious, with strong domain knowledge across therapeutic areas, regulatory standards, and key statistical concepts
  • 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
  • Collaborative team player, skilled at partnering with clients, editors, and scientific leaders
  • Analytical thinker

Nice To Haves

  • Experience working with Medical Affairs and/or Publications deliverables
  • Exposure to commercial content development
  • Familiarity with multiple therapeutic areas or complex disease states

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.
  • Translate complex science into meaningful, impactful communications.
  • Translate data into insights.
  • Interpret results, identify limitations, and communicate insights effectively.

Benefits

  • Growth opportunity
  • Professional development
  • Compensation
  • Health insurance
  • Retirement savings benefits
  • Life insurance
  • Disability benefits
  • Parental leave
  • Paid time off for sick leave and vacation
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