Director, Medical Writing (Hybrid)

Job Description

This is a hybrid position which allows 2 days per week remote work and 3 days per week in our Boston Seaport office. Relocation assistance is available.

The Director, Medical Writing Science has responsibility for the management, oversight, operation, and direction of a group within the department. This role is held accountable for the results of the group and the work performance of line staff and is responsible for setting technical direction for the staff. This role is expected to optimize interdisciplinary understanding and teamwork and integrate activities with those of other groups in Medical Writing Science and with other functions.

Key Duties and Responsibilities:

• Independently authors routine and complex clinical and regulatory documents
• Advises development teams on the content and optimal presentation of documents to facilitate achievement of submission objectives
• Provides strategic input into program-level and therapeutic area plans, including defining the direction of the clinical development program or regulatory strategies
• Sets goals and strategic vision for the group shares that vision within Medical Writing Science
• Optimizes interdisciplinary understanding and synergy within group(s) and integrate activities with those of other department and project teams
• Manages resource plans for projects within their oversight ensuring appropriate staff are available to meet program goals
• Provides coaching and performance management for staff, ensuring goal setting is effectively linked to program and corporate goals
• Plans strategically, anticipates problems, and recommends process improvements to address current and future needs
• Provides expert review of policies and procedures for the department
• innovates and leads process improvements with high cross-functional impact

Knowledge and Skills:

• Highly advanced understanding of the clinical development process and authoring and preparation of the clinical sections of marketing applications and other regulatory submissions
• Proven track record of developing, communicating, and executing strategic direction for projects
• Strong leadership and influencing skills, ability to communicate and present ideas/solutions to senior management
• Ability to recognize business impact and identify networks to gain unified approach to solutions
• Demonstrated knowledge of field
• Ability to manage teams and individuals
• Experience with marketing applications for regulatory submissions

Education and Experience:

• Bachelor's degree in relevant discipline
• Ph.D. (or equivalent degree) highly preferred
• Typically requires 10 years of relevant medical writing experience in Pharma, Biotech or CRO industries and 3 years of supervisory/management experience, or the equivalent combination of education and experience

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Pay Range:

$192,700 - $289,100

Disclosure Statement:

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as: 
1.    Hybrid: work remotely up to two days per week; or select
2.    On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time. 

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