Scientific Content Specialist

Integra Connect; United States; On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Medical/Dental/Vision Insurance

Paid Time Off

401k with employer match

Paid Holidays and Floating Holiday

Job summary

Integra Connect is seeking a Scientific Content Specialist for the Integra PrecisionQ unit to develop high-quality scientific content across publications, market research initiatives, and quality improvement programs. You will collaborate with Medical, Analytics, Quality Initiative, and Commercial Operations to deliver outputs that meet regulatory standards and publication guidelines.

You will support client-facing engagements and internal strategic initiatives, translating complex data into

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); EndNote preferred.
• Travel required (20% - 30%).
• Residence in Eastern or Central U.S. time zones.

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.

Skills

Medical writing

Oncology knowledge

Publication planning

KOL engagement

Regulatory compliance

Education

PhD/MPH/MS in biomedical sciences or related field

Tools

EndNote

MS Office

Job description

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

• 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.Pro
• ficiency 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.

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.