Role Responsibilities
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Draft and develop scientific content (slide decks, summaries, training materials) for pharma and biotech clients.
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Generate outlines and maintain accurate, referenced story arcs.
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Conduct thorough literature searches and data interpretation.
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Organize and annotate references according to client or house style.
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Collaborate with teams in the medical/legal/regulatory (MLR) review process and address committee queries.
Candidate Profile
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Knowledge of multiple therapeutic areas, regulatory/scientific guidelines, and statistical concepts.
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Strong scientific writing skills: logical, succinct, and accurate.
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Skilled in literature review, data interpretation, and recognizing study limitations.
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Highly organized, detail-oriented, and able to meet deadlines.
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Excellent interpersonal and communication skills for problem-solving and teamwork.
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Proficient in Microsoft Word, PowerPoint, Excel, Adobe Acrobat, and reference management software (e.g., EndNote).
About Precision Medicine Group
Precision Medicine Group specializes in scientific and medical communications that transform research into strategies and solutions for clients. With long-standing relationships across pharmaceutical and biotech industries, the company leads in delivering strategic communications, training, and execution support.
Equal Opportunity Employer — decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Applicants needing accommodations may contact: QuestionForHR@precisionmedicinegrp.com.
Note: Precision does not extend job offers without formal interviews. Beware of fraudulent offers not associated with the company.