Director, Medical Writing & Strategy — Hybrid

Vertex Pharmaceuticals; Boston (MA); Híbrido; USD 193.000 - 289.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Relocation assistance

Hybrid work arrangement

Total Rewards benefits

Descripción de la vacante

Vertex is seeking a Director of Medical Writing Science to lead a high-performing group responsible for independently authoring routine and complex clinical and regulatory documents. You will provide strategic input into development and regulatory plans, set the group’s vision, and drive cross-functional collaboration with other teams.

The role emphasizes coaching, resource planning, and process improvements while aligning staff goals with program objectives in a hybrid Boston office

Formación

• Advanced understanding of clinical development and regulatory submissions
• Experience developing and executing strategic direction for projects
• Proven leadership and ability to influence senior management

Responsabilidades

• Independently authors routine and complex clinical and regulatory documents
• Advises development teams on content and presentation to meet submission objectives
• Provides strategic input into program-level plans and regulatory strategies
• Sets goals and strategic vision for the group and shares it across Medical Writing Science
• Optimizes cross-functional understanding within the group and with other departments
• Manages resource plans to meet program goals
• Coaches staff and links goals to program and corporate objectives
• Plans strategically, anticipates problems, and recommends improvements
• Reviews policies and procedures for the department
• Leads process improvements with cross-functional impact

Conocimientos

Clinical development

Regulatory writing leadership

Cross-functional collaboration

Strategic direction

Staff coaching

Communication to senior management

Educación

Bachelor's degree in relevant discipline

Ph.D. (or equivalent) preferred

Descripción del empleo

Vertex is seeking a Director of Medical Writing Science to lead a high-performing group responsible for independently authoring routine and complex clinical and regulatory documents. You will provide strategic input into development and regulatory plans, set the group’s vision, and drive cross-functional collaboration with other teams.

The role emphasizes coaching, resource planning, and process improvements while aligning staff goals with program objectives in a hybrid Boston office