Associate Director – Medical Affairs, Publications
Braveheart Bio
Posted: 10/21/2026
Associate Director, Clinical Trial Management
Syneos Health
Posted: 10/21/2026
Director, Clinical and Regulatory Strategic Communications
MSD
Posted: 10/21/2026
Associate Director, Clinical Supply Management
Novartis
Posted: 10/21/2026
Medical Director – National OP, Medicare
Humana
Posted: 10/21/2026
Field Medical Director, Breast and Gynecological Cancers – Non-MD
Pfizer
Posted: 10/21/2026Field Medical Director, Breast and Gynecological Cancers
Pfizer
Posted: 10/21/2026
Associate Medical Director, Rare Disease – Friederichs Ataxia
Biogen
Posted: 10/21/2026
Project Director – Clinical Study Management
Alimentiv
Posted: 10/21/2026Field Medical Director, Breast and Gynecological Cancers
Pfizer
Posted: 10/21/2026Field Medical Director, Breast and Gynecological Cancers – Non-MD
Pfizer
Posted: 10/21/2026
Director, Clinical Chargemaster
Mercy
Posted: 10/21/2026Senior Director, Clinical Science, Thoracic Oncology
MSD
Posted: 10/21/2026Senior Director, Clinical Science, Genitourinary (GU) Oncology
MSD
Posted: 10/21/2026Senior Director, Clinical Science, Gastrointestinal – Oncology
MSD
Posted: 10/21/2026Senior Director, Clinical Science, Breast Oncology
MSD
Posted: 10/21/2026Senior Director, Clinical Science, Gynecologic Oncology
MSD
Posted: 10/21/2026
Medical Director – Oncology
CTI Clinical Trial and Consulting Services
Posted: 10/21/2026
Medical Director, Gastroenterology
ModMed
Posted: 10/21/2026
Associate Scientific Director – Medical Communications
Avalere
Posted: 10/21/2026Associate Director – Medical Affairs, Publications
Braveheart BioPosted 10/21/2026full-timeRemote • California • United StatesSenior💰 $175,000 - $245,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in strategic publication planning and execution, with a strong focus on compliance with GPP, ICMJE, and CONSORT guidelines. Proven ability to manage cross-functional collaborations and lead publication initiatives in the biotech and pharmaceutical sectors.
Highest-signal resume keywords
Strategic Publication PlanningScientific Writing and EditingClinical Trial Design UnderstandingProject Management SkillsExperience in Biotech/Pharma
About the role
Key responsibilities & impact- Own the publications function for BHB-1893
- Lead strategy, planning, and execution of a multi-year publication and congress plan
- Drive publications from concept through submission and publication
- Develop and maintain the integrated strategic publication plan and publication concept backlog
- Identify and prioritize clinical, clinical pharmacology, nonclinical, mechanistic, HEOR, disease-state, review, and real-world evidence opportunities
- Define journal and congress targeting strategies
- Lead abstracts, posters, oral presentations, and manuscripts for cardiovascular and HCM congresses
- Manage submission calendars, deadlines, data readouts, and topline disclosures
- Monitor competitive readouts and the external scientific landscape
- Coordinate with Clinical Development, Biostatistics, Clinical Operations, Clinical Pharmacology, Regulatory, HEOR, Legal, Compliance, Commercial, and licensing partner Hengrui Pharma
- Engage investigators, steering committee members, and external authors
- Develop and maintain reactive scientific content including slide decks, FAQs, and standard response documents
- Build publications infrastructure, SOPs, steering committee, workflows, and publication management system
- Ensure compliance with GPP, ICMJE, CONSORT, company policies, authorship, disclosures, transparency, and audit documentation
- Manage publication and medical writing agencies, budgets, timelines, and quality
- Track publication metrics and report progress
- Contribute to advisory boards, scientific training, and medical communications as needed
- Reports to the Head of Medical Affairs
Requirements
What you’ll need- Advanced scientific degree (MD, PhD, PharmD, or equivalent)
- Associate Director: 5+ years of publications or scientific communications experience in biotech/pharma or a medical communications agency
- Director: 8+ years of experience, including leading publication strategy for a late-stage or launch asset
- Proven experience with strategic publication planning and execution across all phases of drug development
- In-depth knowledge of GPP, ICMJE, CONSORT, and related guidance
- Understanding of clinical trial design, statistical methods, and clinical data reporting
- Experience working in a matrixed, cross-functional environment and influencing without authority
- Strong scientific writing, editing, and data interpretation skills
- Experience managing external agencies, authors, and budgets
- Strong organizational and project management skills
- Ability to work independently and collaboratively in a fast-moving, resource-lean environment
- Ability to travel domestically and internationally approximately 15–20%
- E-Verify employment authorization confirmation for new hires
- Preferred: cardiovascular medicine/HCM background, CMPP certification, late-breaking presentations and simultaneous publications, global publications with ex-US or licensing partners, publications-function building, HEOR/RWE and clinical pharmacology publications, publication management platforms
Benefits
Comp & perks- Annual bonus eligibility
- Equity eligibility
- Comprehensive benefits offering
- Ability to work remotely or in a hybrid arrangement
- Equal opportunity and inclusion-focused workplace
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Publication StrategyData InterpretationClinical Data ReportingBudget ManagementPublication Metrics TrackingAbstract and Manuscript DevelopmentCongress Targeting StrategiesPublication Infrastructure DevelopmentCompliance with GPPHEOR and RWE Publications
Soft Skills
Strong Organizational SkillsAbility to Work IndependentlyCollaborative TeamworkInfluencing Without AuthorityAdaptability in Fast-Moving Environments
Tools & Technologies
Publication Management PlatformsPublication Management SystemScientific Content Development Tools
Certifications & Qualifications
CMPP Certification
Industry Keywords
BiotechPharmaceuticalMedical CommunicationsCardiovascular MedicineHCMClinical PharmacologyRegulatory ComplianceScientific TrainingAdvisory BoardsLate-Stage Drug Development