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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Medical Writing Manager

Technical WritingConfirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • Experience writing and editing clinical regulatory documents.
  • Ability to analyze, interpret, and summarize moderately complex data.
  • Broad understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory requirements, and medical terminology.
  • Ability to manage project teams, form productive working relationships, and work through conflicts.
  • Excellent project management and organizational skills.
  • Ability to complete work resourcefully and independently, design alternative approaches, and use guidance and mentoring on new or complex issues.
  • Initiative and creativity in solving routine problems affecting multiple documents and contributing to cross-functional process improvements.
  • Advanced computer skills related to word processing, templates, table and figure creation, literature searches, electronic review systems, and document management systems; ability to serve as a resource for others using these tools.
  • Ph.D. or equivalent degree.
  • Typically requires 4 years of experience or an equivalent combination of education and experience.

Responsibilities

  • Author moderately complex clinical regulatory documents, including clinical study protocols, clinical study reports, investigator’s brochures, and sections of regulatory submissions, in partnership with key cross-functional stakeholders.
  • Serve as the lead Medical Writing Scientist for moderately complex clinical studies.
  • Support the Medical Lead with review and interpretation of clinical study data and respond to questions from study team members.
  • Participate in developing key messages for moderately complex clinical regulatory documents.
  • Ensure medical and scientific consistency between related documents or studies in a clinical program.
  • Analyze and interpret data thoroughly and critically to determine the best approach to composing each document.
  • Contribute scientific input, information from previous studies, and data integration and review to product development plans, and serve as coordinating author for those plans.
  • Participate in developing standard operating processes and related procedures.

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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