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Syneos Health

Publications and Scientific Communications Writer – Principal/Sr Principal

Syneos Health

. Lead development and implementation of portfolio asset/product publication strategy and plans .

Posted 10/16/2026full-timeRemote • United StatesSenior💰 $95,000 - $175,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing publication strategies and scientific communication within the pharmaceutical industry, with a strong focus on project management, writing, and compliance with publication practices. Proficient in collaborating with cross-functional teams and external stakeholders to produce high-quality scientific publications.

Highest-signal resume keywords
Publication Strategy DevelopmentProject Management SkillsScientific Writing ExperienceCross-Functional Stakeholder ManagementFamiliarity With Publication Planning Software

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Scientific WritingPublication ManagementClinical Development UnderstandingData AnalysisBudget PlanningMultitaskingAttention to DetailCritical Appraisal of LiteratureOncology ExperienceDermatology Experience
Soft Skills
Interpersonal SkillsLeadershipEffective CommunicationTeam CollaborationAbility to Work Independently
Tools & Technologies
Microsoft OfficeIEnvisionLiterature Search IndicesJournal Databases
Certifications & Qualifications
Advanced Degree in Scientific Discipline
Industry Keywords
Pharmaceutical IndustryMedical CommunicationPublication PracticesScientific ConferencesPeer-Reviewed Journals

About the role

Key responsibilities & impact
  • Lead development and implementation of portfolio asset/product publication strategy and plans
  • Produce high-quality publications
  • Contribute to disease or product scientific platform/statements strategy and development
  • Lead discussions with external authors and collaborators across Medical Affairs, Drug Development, and Drug Discovery organizations
  • Manage external agencies and freelancers involved in writing, editing, formatting, and submitting articles to peer-reviewed journals and scientific/medical conferences
  • Manage publication reviews with authors, reviewers, and external authors
  • Track and report publication development progress using appropriate software to catalogue project status, drafts, comments, and approvals
  • Write, edit, and format primary manuscripts, congress abstracts, slide presentations, and posters
  • Manage budget planning and milestones
  • Follow authorship guidelines and good publication practices
  • Ensure medical/scientific publication activities comply with company policies, procedures, and good publication practices
  • Contribute to maintenance and rollout of departmental policies
  • Travel primarily in the U.S. and Europe for scientific conferences, less than 10% of the time

Requirements

What you’ll need
  • Advanced degree in a scientific discipline (e.g., PhD, PharmD)
  • Minimum 5 years of experience within the pharmaceutical industry, a medical communication company, or a consulting organization, as a publication manager or senior level content reviewer
  • Writing experience is essential
  • Exceptional project management skills
  • Demonstrated leadership in running a publication strategy and plan, and developing scientific platforms
  • Ability to plan, prioritize, and execute multiple projects; multitask and work independently and within multi-disciplinary teams
  • Understanding of the clinical development process, especially clinical study data and outcomes measures
  • Ability to critically appraise and apply knowledge from medical/scientific literature
  • High attention to detail and scientific rigor
  • Strong interpersonal skills for effective professional communications
  • Demonstrated leadership and cross-functional stakeholder management skills
  • Ability to effectively communicate complex medical/scientific information and contribute to medical strategy
  • Ability to respond to urgent timelines
  • Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook
  • Familiarity and working knowledge of publication planning and implementation software, including iEnvision, literature search indices, and journal databases
  • Experience in oncology and/or dermatology is a plus
  • Travel estimated at less than 10% of time

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • Company car or car allowance
  • Medical, Dental and Vision health benefits
  • Company match 401k
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO)
  • Sick time
  • Reasonable accommodations, when appropriate