3 часа назад
Associate Scientific Communications Director (Biotechnology)
165 000 - 214 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Scientific Communications Director (Biotechnology): Developing and executing scientific communications strategies across a clinical-stage biotechnology portfolio with an accent on publication planning, congress execution, and compliant scientific content. Focus on translating clinical and translational data into clear narratives, coordinating cross-functional stakeholders, and managing complex publication timelines under GPP2022 and ICMJE standards.
Location: Boston, Massachusetts, United States; hybrid schedule with at least two on-site days per week, currently Tuesday and Wednesday
Salary: $165,000–$214,500 USD per year, plus potential discretionary annual bonus and long-term incentive award.
Company
is a clinical-stage biotechnology company developing precision therapies for autoimmune and inflammatory diseases.
What you will do
- Develop and execute scientific communications plans aligned with asset strategy and medical affairs objectives.
- Manage global publication activities, including author engagement, abstracts, manuscripts, posters, and oral presentations.
- Coordinate content development and internal alignment for major international and regional medical congresses.
- Draft and edit scientific materials such as slide decks, scientific exchange content, FAQs, and Field Medical training resources.
- Maintain publication trackers and timelines while managing vendor and agency relationships for on-time, on-budget delivery.
- Support advisory boards, investigator meetings, external scientific forums, and the development of consistent compliant communication standards.
Requirements
- PhD, PharmD, MS, or equivalent advanced scientific degree.
- 7+ years of experience in scientific communications, medical affairs, or related biotech or pharmaceutical roles.
- Experience with publication strategy and congress execution, ideally for Phase 2/3 or Phase 3 programs.
- Strong knowledge of scientific publication standards, data disclosure requirements, and medical compliance, including GPP2022 and ICMJE guidelines.
- Excellent scientific writing, project management, organizational, communication, and independent problem-solving skills.
- Ability to work on-site in Boston at least two days per week.
Nice to have
- Experience in autoimmune, immunology, or inflammatory diseases.
Culture & Benefits
- Fast-paced, evolving, and resource-constrained biotechnology environment.
- Collaboration across Clinical Development, Regulatory, Commercial, and Medical Affairs.
- Health and wellness coverage, with benefits tailored to the hiring country or region.
- Paid time off, public holidays, and additional leave according to local requirements.
- Flexible work arrangements within the hybrid schedule.
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