Scientific Content Specialist

Job Description

Company Summary:

We are a value-based, precision medicine company specializing in Health IT, real-world data, and digital health solutions for specialty providers, payers, and life sciences companies.Through the provision of technology products and technology-enabled services, along with unmatched clinical expertise, we are able to close gaps in care, improve patient outcomes, generate real-world evidence, and accelerate and augment customer commercial success across the healthcare value chain. We are looking for like-minded individuals committed to making a difference in healthcare. Come join our growing team!

Job Description:

The 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 Scientific Content Specialist will support client-facing engagements and internal strategic initiatives while ensuring scientific accuracy, regulatory compliance, and alignment with publication standards.

Responsibilities:

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• Develop scientific publications including abstracts, posters, manuscripts, and conference presentations for submission to peer-reviewed journals and medical conferences.
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• Support market research initiatives by developing materials for advisory boards, market insights meetings, and stakeholder engagement sessions.
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• Create discussion guides, slide decks, and summary reports synthesizing insights from expert advisory panels and market research activities.
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• Collaborate with Medical, Analytics, Quality Initiative, and Commercial Operations teams to translate complex data and clinical findings into clear, compelling narratives for diverse audiences.
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• Partner with internal teams to develop content for internal communications, training materials, and strategic planning documents.
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• Conduct literature reviews and synthesize scientific evidence to support publication strategies and market research objectives.
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• Support the Commercial Operations team by developing protocols, standard operating procedures, best practice guidelines, and implementation toolkits.
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• Manage multiple writing projects simultaneously while meeting tight deadlines and maintaining high-quality standards.
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• Ensure all deliverables comply with Current Good Publication Practice (cGPP) guidelines, journal requirements, and regulatory standards.
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• Participate in client meetings and presentations as needed to support project delivery and relationship development.
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• Strategically consider how content for healthcare providers and life science companies can be collaborated for strategic purposes.
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Qualifications:

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• Advanced degree in biomedical sciences, public health, epidemiology, or a related field (PhD, MPH, or MS preferred).
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• 3-5 years of medical writing experience in healthcare, life sciences, pharmaceutical, or biotechnology settings.
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• 1-2 years of experience in creating oncology-specific deliverables.Pro
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• ficiency in ICJME best practices and ethical standards in reporting research in medical publications.
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• Demonstrated experience developing scientific publications (abstracts, posters, manuscripts) for peer-reviewed journals and medical conferences.
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• Experience supporting advisory boards, KOL engagements, or market research activities.
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• Oncology expertise from a scientific, medical, or pharmaceutical background with a basic understanding of the mechanism of oncology, and common therapies.
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• Experience with Current Good Publication Practice (cGPP) guidelines, publication ethics standards, and ICMJE authorship criteria.
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• Strong project management skills with ability to handle multiple concurrent projects and prioritize effectively.
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• Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel); experience with reference management software (EndNote) preferred.
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• Preferred qualities: pro-active, collaborative, creative, energetic, and positive.
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• Travel required (20% - 30%)
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• This position requires candidates to reside in either the Eastern or Central U.S. time zones.
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Benfits:

Integra Connect, LLC provides a comprehensive benefits plan

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• Medical/Dental/Vision Insurance beginning the 1st of the month following your date of hire
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• Paid Time Off
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• 401k with employer match
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• Paid Holidays and Floating Holiday
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Equal Opportunity Employer

Please note that the deadline for submitting applications is October 31, 2026. All applications must be received by this date to be considered.