Associate Director – Medical Affairs, Publications

🔥 10 hours ago

🏄 California – Remote

🏄 California – Remote

💵 $175k - $245k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

👻 Ghost score 15%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Braveheart Bio

WebsiteLinkedInAll Job Openings

1 - 10 employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Braveheart Bio is a clinical-stage biotechnology company focused on transforming the care of hypertrophic cardiomyopathy (HCM) and related conditions. The company is developing investigational therapies that selectively target overactive myosin — a key disease mechanism in HCM — and is advancing a program through global late-stage (Phase 3) clinical development to improve heart performance and patient quality of life.

📋 Description

• 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

• 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

• Annual bonus eligibility • Equity eligibility • Comprehensive benefits offering • Ability to work remotely or in a hybrid arrangement • Equal opportunity and inclusion-focused workplace