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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Director Medical Writing

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • Bachelor's degree in a relevant discipline.
  • Typically requires 10 years of relevant medical writing experience in the pharmaceutical, biotechnology, or contract research organization industries and 3 years of supervisory or management experience, or an equivalent combination of education and experience.
  • Highly advanced understanding of the clinical development process and authoring and preparation of clinical sections of marketing applications and other regulatory submissions.
  • Proven track record of developing, communicating, and executing strategic direction for projects.
  • Ability to communicate and present ideas and solutions to senior management.
  • Ability to recognize business impact and identify networks to gain a unified approach to solutions.
  • Demonstrated knowledge of the field.
  • Ability to manage teams and individuals.
  • Experience with marketing applications for regulatory submissions.

Responsibilities

  • Independently author routine and complex clinical and regulatory documents.
  • Advise development teams on document content and optimal presentation to facilitate achievement of submission objectives.
  • Provide strategic input into program-level and therapeutic-area plans, including defining the direction of clinical development programs or regulatory strategies.
  • Set goals and strategic vision for the group and share that vision within Medical Writing Science.
  • Optimize interdisciplinary understanding and synergy within groups and integrate activities with other departments and project teams.
  • Manage resource plans for projects under oversight, ensuring appropriate staff are available to meet program goals.
  • Provide coaching and performance management for staff, ensuring goal setting is effectively linked to program and corporate goals.
  • Plan strategically, anticipate problems, and recommend process improvements to address current and future needs.
  • Provide expert review of departmental policies and procedures.
  • Innovate and lead process improvements with high cross-functional impact.

Desired Qualifications

  • A Ph.D. or equivalent degree is highly preferred.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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