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About You:
- Domain knowledge of multiple therapeutic areas, regulatory/scientific guidelines, and key statistical concepts.
- Excellent writing skills, are logical and succinct with accurate data interpretation.
- Highly organized, dedicated, respects metrics driven timelines.
What You Can Expect Day-to-Day:
- Generate content outlines that contain a clearly highlighted story arc and a complete reference list.
- Develop client-ready drafts of content in various forms (slide decks, summaries, materials).
- Confer with teams in the medical/legal/regulatory (MLR) review process.
Qualifications:
- Advanced Science Degree (PharmD, MD, PhD) and 0-3 years of relevant experience.
- Proficiency in using Microsoft Word®, PowerPoint®, Excel®, Adobe Acrobat®, and reference-management software (e.g. EndNote®).
- Experience in content reviews; correctly interprets results, identify potential limitations, and discusses unexpected findings.
Precision Medicine Group
Precision Medicine Group translates the science of medicine into high-level strategy, tactical communication, and flawless execution. They have long-tenured relationships with major pharmaceutical companies and leading biotech firms, holding a leadership position in strategic medical communication and training solutions.