Contractor, Global Scientific Communications

PTC Therapeutics, Inc.

. Support development and lead tactical execution of Publication and Medical Education plans aligned with asset strategy and medical affairs objectives .

Posted 11/9/2026full-timeRemote • United StatesMid-LevelSenior💰 $80 - $130 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Scientific Publications and Medical Education, with a strong understanding of publication standards and compliance. Proven ability to manage complex projects and collaborate effectively across cross-functional teams in the biopharmaceutical industry.

Highest-signal resume keywords

Scientific Publications ExpertiseMedical Education Best PracticesProject Management SkillsAdvanced Medical DegreeKnowledge of GPP4 and ICMJE Guidelines

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Publication PlanningScientific ReviewData Disclosure RequirementsClinical Trial DesignStatistical Methods

Soft Skills

Excellent Communication SkillsInfluencing Without AuthorityOrganizational SkillsCollaboration SkillsIndependent Work

Tools & Technologies

Microsoft Office SuitePubstratVeeva MedCommsVideo Conferencing Platforms

Certifications & Qualifications

Advanced Medical or Scientific Degree (MD, PharmD, PhD, MS, MPH)

Industry Keywords

Biopharmaceutical IndustryHealthcareMedical AffairsOrphan DiseasesGenetic Disorders

About the role

Key responsibilities & impact

Support development and lead tactical execution of Publication and Medical Education plans aligned with asset strategy and medical affairs objectives
Execute publication planning and publication development
Manage global publication activities, including author engagement, abstracts, manuscripts, posters, and oral presentations, in compliance with GPP and company SOPs
Serve as scientific lead and reviewer for publication deliverables, identifying data gaps, inconsistencies, and interpretation risks and driving resolution with cross-functional SMEs
Oversee plans and activities for major international and regional medical meetings, including content development and internal alignment
Own scientific content, including slide decks, scientific exchange materials, and FAQs for Field Medical teams
Partner with cross-functional teams to ensure accurate interpretation and timely dissemination of data
Maintain publication trackers, timelines, and vendor/agency relationships for on-time, on-budget delivery
Support advisory boards, investigator meetings, and external scientific forums
Assist in establishing processes and standards for consistency and compliance across scientific materials
Keep internal colleagues informed of Publications and Medical Education activities
Manage agency partner performance
Provide scientific review of Scientific Communications materials
Cooperate with Global Medical functions and Regional Medical teams
Contribute to Medical Education and Publications best practices, standards, and systems
Collect and provide metrics measuring medical education programs and scientific publications
Support planning and management of the Scientific Communications budget
Maintain and expand therapeutic-area, disease, and product knowledge

Requirements

What you’ll need

An advanced medical or scientific degree (MD, PharmD, PhD, MS, MPH) is required
5+ years of experience in Biopharmaceutical/Healthcare industry, preferably within a matrix structure and within Scientific Communications roles
Relevant experience in other Medical Affairs roles (e.g. Medical Science Liaison, Medical Information) will be considered
Expertise in Scientific Publications, including planning and execution across phases of drug development and commercialization
Deep knowledge of scientific publication standards, data disclosure requirements, and medical compliance, including GPP4 and ICMJE guidelines is required
Expertise in Medical Education approaches and best practices is required
Experience in orphan/rare diseases, molecular biology, metabolic disorders, neurology and/or genetic disorders
In-depth knowledge of Good Publication Practices (GPP4), ICMJE, CONSORT, Sunshine Act, relevant Codes of Conduct (e.g. PhRMA, EFPIA), and post-marketing practices and scientific data communication
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements
Demonstrated expertise in Publications planning and development and implementation of Scientific Publications
Excellent project management and organizational skills, with ability to manage multiple concurrent projects and timelines
Excellent verbal and written communication skills; ability to influence without authority
Demonstrated experience working independently and collaboratively in a fast-paced, matrixed, team environment
Proficiency with Microsoft Office Suite, Publications and Medical materials management platforms (e.g. Pubstrat, Veeva MedComms), and video conferencing platforms
People and project management experience
Fluent in English (verbal and written)
5-15% travel