[Remote] Scientific Content Specialist

Note: The job is a remote job and is open to candidates in USA. Integra Connect is a value-based, precision medicine company specializing in Health IT and digital health solutions. The Scientific Content Specialist will develop high-quality scientific content and collaborate with cross-functional teams to support life sciences and diagnostics industry partners.

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

• 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
• Travel required (20% - 30%)
• This position requires candidates to reside in either the Eastern or Central U.S. time zones
• Pro-active, collaborative, creative, energetic, and positive

Benefits

• 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

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