Associate Director, Global Scientific Communications, Medical Affairs
J
JobgetherBiotechnology, Pharmaceuticals
Remote work opportunity within the United States.Full-TimeDirector
Salary not disclosed
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Job Details
- Experience
- 5+ years
- Required Skills
- Project Management
Requirements
- Advanced degree in life sciences such as PhD, PharmD, MD, MS, or equivalent.
- 5+ years of experience in medical communications, scientific writing, or content development within biotechnology, pharmaceutical, or healthcare organizations.
- Strong understanding of Medical Affairs functions, processes, and industry standards.
- Proven ability to synthesize complex scientific information and tailor communication for different audiences.
- Exceptional writing, editing, presentation, and verbal communication skills.
- Experience managing multiple projects simultaneously while balancing competing priorities.
- Strong project management skills with experience overseeing agencies, vendors, and external collaborators.
- Ability to work independently and operate effectively in a fast-paced, matrixed environment.
- Experience with content management and review platforms such as Veeva Vault or similar systems.
- Familiarity with scientific communication compliance standards including ICMJE, GPP, FDA, and EMA guidelines.
- Scientific background or experience in oncology, hematology, autoimmune diseases, or related therapeutic areas is preferred.
Responsibilities
- Develop and execute global scientific communication strategies, messaging frameworks, and content plans for key therapeutic assets.
- Create high-quality scientific materials including presentations, slide decks, scientific narratives, FAQs, congress materials, and publication-related content.
- Translate complex clinical and scientific data into accurate, engaging, and compliant communications.
- Support publication planning and execution, including abstracts, posters, manuscripts, and scientific presentations.
- Collaborate with healthcare professionals, authors, agencies, and internal stakeholders to ensure alignment of scientific messaging.
- Drive innovative approaches to scientific communication through digital formats and enhanced content delivery.
- Partner with cross-functional teams including Clinical Development, Regulatory, and Commercial functions.
- Manage content development projects, timelines, budgets, and external vendor relationships.
- Oversee review and approval processes through content management platforms while ensuring compliance.
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