The job, in the employer's words
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 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.
About You:
- 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
About the Role:
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 Experience:
- 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
Helpful Experience:
- Experience working with Medical Affairs and/or Publications deliverables
- Exposure to commercial content development
- Familiarity with multiple therapeutic areas or complex disease states
Who We Are
Precision AQ - Medical Communications was founded with the simple belief that the scientific story is the foundation of every pharmaceutical brand. Our teams of inquisitive problem solvers and passionate creators dig deep to translate the science behind today’s cutting-edge therapies, then communicate the science clearly and credibly. Our proven track record of long-tenured relationships with major pharmaceutical companies and leading bio-tech firms, and our inclusive, open-minded team culture are industry leading. This passionate work environment, paired with growth opportunity, professional development, compensation, and benefits, are why Precision AQ - Medical Communications was recognized as a Best Place to Work by the Philadelphia Business Journal for the last three years.
Are you ready to join a team committed to providing the best in science and strategy?
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
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Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Requirements mentioned
- 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
- About the Role: 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.
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