Scientific Content Specialist at Integra Connect

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: • 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. • 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 October 31, 2026. All applications must be received by this date to be considered.

Requirements

Must-haves

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.
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.
Travel required (20% - 30%)

Nice-to-haves

Advanced degree in biomedical sciences, public health, epidemiology, or a related field (PhD, MPH, or MS preferred).
Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel); experience with reference management software (EndNote) preferred.
Preferred qualities: pro-active, collaborative, creative, energetic, and positive.

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: paycom
Effort: medium

Benefits

Benefits detected in the listing.

Dental

Vision

401k

Paid Time Off