Scientific Content Specialist

## Job DescriptionThe Scientific Content Specialist will be a key member of the Integra PrecisionQ business unit. The individual will be responsible for developing high-quality scientific content across publications, market research initiatives, and quality improvement programs. This role requires collaboration with cross-functional teams including Medical, Analytics, Quality Initiative, and Commercial Operations to deliver exceptional outputs for our life sciences and diagnostics industry partners. The Manager of Scientific Content will support client-facing engagements and internal strategic initiatives while ensuring scientific accuracy, regulatory compliance, and alignment with publication standards.**Responsibilities:*** Develop scientific publications including abstracts, posters, manuscripts, and conference presentations for submission to peer-reviewed journals and medical conferences.* Support market research initiatives by developing materials for advisory boards, market insights meetings, and stakeholder engagement sessions.* Create discussion guides, slide decks, and summary reports synthesizing insights from expert advisory panels and market research activities.* Collaborate with Medical, Analytics, Quality Initiative, and Commercial Operations teams to translate complex data and clinical findings into clear, compelling narratives for diverse audiences.* Partner with internal teams to develop content for internal communications, training materials, and strategic planning documents.* Conduct literature reviews and synthesize scientific evidence to support publication strategies and market research objectives.* Support the Commercial Operations team by developing protocols, standard operating procedures, best practice guidelines, and implementation toolkits.* Manage multiple writing projects simultaneously while meeting tight deadlines and maintaining high-quality standards.* Ensure all deliverables comply with Current Good Publication Practice (cGPP) guidelines, journal requirements, and regulatory standards.* Participate in client meetings and presentations as needed to support project delivery and relationship development.* Strategically consider how content for healthcare providers and life science companies can be collaborated for strategic purposes.## Qualifications* Advanced degree in biomedical sciences, public health, epidemiology, or a related field (PhD, MPH, or MS preferred).* 3-5 years of medical writing experience in healthcare, life sciences, pharmaceutical, or biotechnology settings.* 1-2 years of experience in creating oncology-specific deliverables.* Proficiency in ICJME best practices and ethical standards in reporting research in medical publications.* Demonstrated experience developing scientific publications (abstracts, posters, manuscripts) for peer-reviewed journals and medical conferences.* Experience supporting advisory boards, KOL engagements, or market research activities.* Oncology expertise from a scientific, medical, or pharmaceutical background with a basic understanding of the mechanism of oncology, and common therapies.* Experience with Current Good Publication Practice (cGPP) guidelines, publication ethics standards, and ICMJE authorship criteria.* Strong project management skills with ability to handle multiple concurrent projects and prioritize effectively.* Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel); experience with reference management software (EndNote) preferred.* Preferred qualities: pro-active, collaborative, creative, energetic, and positive.* Travel required (20% - 30%)* This position requires candidates to reside in either the Eastern or Central U.S. time zones.**Benefits:***Integra Connect, LLC provides a comprehensive benefits plan** Medical/Dental/Vision Insurance beginning the 1st of the month following your date of hire* Paid Time Off* 401k with employer match* Paid Holidays and Floating Holiday*Equal Opportunity Employer***Please note that the deadline for submitting applications is April 30, 2026. All applications must be received by this date to be considered.**
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