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Associate Director, Global Publications
Encoded Therapeutics Inc.. Lead the development, alignment, and execution of comprehensive global publication plans across preclinical and clinical assets.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in medical writing and scientific communications within the biotechnology or pharmaceutical industry, with a strong understanding of publication processes and compliance standards. Capable of managing publication plans, collaborating with cross-functional teams, and effectively communicating complex scientific information.
Highest-signal resume keywords
Medical Writing ExperienceScientific Publication ProcessesProject Management SkillsCollaboration Across TeamsRegulatory Compliance Knowledge
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Scientific WritingData CommunicationStatistical MethodsMedical TerminologyPublication Management
Soft Skills
Attention to DetailInterpersonal SkillsOrganizational SkillsAdaptabilityEmpathetic Communication
Tools & Technologies
Publication Management SoftwareWordExcelPowerPointAdobe Presentation Tools
Certifications & Qualifications
PhDMaster's DegreeBachelor's Degree
Industry Keywords
BiotechnologyPharmaceuticalMedical CommunicationsGene TherapyNeuroscience
About the role
Key responsibilities & impact- Lead the development, alignment, and execution of comprehensive global publication plans across preclinical and clinical assets.
- Drive end-to-end development of peer-reviewed manuscripts, congress abstracts, posters, and oral presentations.
- Collaborate with Clinical Development/Sciences, Biometrics, Translational Research, Regulatory Affairs, and Medical Affairs.
- Establish and manage program-specific Publication Steering Committees and author working groups.
- Facilitate authorship meetings, consensus-building, and data disclosure reviews.
- Manage external medical communications agencies, scientific writers, and graphics vendors.
- Ensure publication deliverables comply with company policies, Good Publication Practice guidelines, ICMJE recommendations, and applicable regulatory standards.
- Oversee publication management software and tools for submission tracking, MLR reviews, author agreements, and archival processes.
- Contribute to strategic congress planning and coordinate publication disclosures aligned with key scientific congresses.
- Oversee scientific session coverage, presentation logistics, and post-congress scientific debriefs.
- Support Patient Advocacy and HEOR publications as needed.
- Travel internationally and domestically as required.
- Report to the Director, Scientific Communications.
Requirements
What you’ll need- A minimum of twelve years of related experience with a Bachelor’s degree; or eight years and a Master’s degree; or a PhD with three to five years of experience; or equivalent experience.
- Three to five years of medical writing, publications, or scientific communications experience within the biotechnology/pharmaceutical industry or a medical communications agency.
- Strong understanding of scientific publication processes, data communication, medical terminology, statistical methods, and compliance principles.
- Proven ability to draft clear, concise scientific content and translate technical data for diverse audiences.
- Excellent writing, editing, and project management skills with strong attention to detail.
- Highly organized with the ability to manage multiple deliverables concurrently under standard supervision.
- Collaborative team player with strong interpersonal skills and comfort working across cross-functional teams.
- Ability to communicate complex scientific information empathetically with patient communities.
- Flexible, adaptable, and comfortable working in a dynamic, fast-paced environment.
- Proficiency in Word, Excel, PowerPoint, and Adobe presentation tools.
- Preferred: advanced degree (PhD, PharmD, or MD) in a life science field.
- Preferred: experience in gene therapy, epilepsy, neuroscience, or rare disease.
- Preferred: knowledge of digital and multimedia scientific communication formats.
- Preferred: comfort with graphic design and video editing tools.
Benefits
Comp & perks- Discretionary annual bonus
- Discretionary stock-based long-term incentives
- Paid time off
- Comprehensive benefits package, including competitive employer premium contributions
- Meaningful stock option grants
- Sick time and holiday pay
- Generous Parental Leave program
- Pre-tax medical and dependent care programs
- Short-term disability, long-term disability, life and AD&D insurance
- Professional development opportunities
- Team-building events
- Fully stocked micro-kitchen
- Fitness center at South San Francisco location