Senior Associate Director, Scientific Communications

BioSpace; Cambridge (MA); Híbrido; USD 165.000 - 215.000; Tempo integral

Benefícios oferecidos por esta vaga

Health and wellness coverage

Paid time off

Flexible hybrid work

Resumo da vaga

Beeline Medicines seeks an Associate Director of Scientific Communications to lead the publication strategy across the portfolio, translating clinical data into high-quality materials for internal and external audiences. You will drive day-to-day publication planning and congress activities, partnering with Clinical Development, Regulatory, Medical Affairs, and Commercial teams.

The role requires expert scientific writing, strong project management, and comfort working in a fast-paced biotech

Qualificações

• PhD/PharmD/MS or equivalent required.
• 7+ years in scientific communications or related biotech roles.
• Experience supporting publication strategy and congress execution for late-stage programs.

Responsabilidades

• Support development and lead execution of the scientific communications plan.
• Manage global publication activities (abstracts, manuscripts, posters, talks).
• Oversee plans for major international/regional medical meetings.
• Draft and edit scientific content for Field Medical teams.
• Collaborate with cross-functional teams to interpret data timely.
• Maintain publication trackers and vendor relationships.
• Support advisory boards and investigator meetings.
• Establish processes to ensure consistency and compliance.

Conhecimentos

Scientific writing

Project management

Cross-functional collaboration

Publication planning

Regulatory compliance

Formação

PhD, PharmD, MS, or equivalent advanced scientific degree

Descrição da vaga

Beeline Medicines seeks an Associate Director of Scientific Communications to lead the publication strategy across the portfolio, translating clinical data into high-quality materials for internal and external audiences. You will drive day-to-day publication planning and congress activities, partnering with Clinical Development, Regulatory, Medical Affairs, and Commercial teams.

The role requires expert scientific writing, strong project management, and comfort working in a fast-paced biotech