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Oncology Regulatory Lead: Senior Principal Medical Writer

Syneos Health, Inc.

Greater London

On-site

GBP 85,000 - 158,000

Full time

Yesterday
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Job summary

A leading biopharmaceutical solutions organization is seeking a Senior Principal Medical Writer to develop regulatory documents and manage writing projects. This role involves collaboration with cross-functional teams to ensure timely delivery of quality documents. The ideal candidate will have an advanced degree in life sciences and experience with global regulatory submissions. Join us to help improve patients’ lives with innovative therapies.

Benefits

Health benefits including Medical, Dental, Vision
401k company match
Eligibility for Employee Stock Purchase Plan
Flexible paid time off

Qualifications

  • Experience with global regulatory submissions.
  • Strong understanding of ICH guidelines.
  • Ability to mentor junior medical writers.

Responsibilities

  • Develop regulatory documents for submissions to agencies globally.
  • Manage timelines and communication with cross-functional teams.
  • Mentor junior writing staff.

Skills

Regulatory document development
Project management
Team collaboration

Education

Advanced degree in life sciences or related field
Job description
A leading biopharmaceutical solutions organization is seeking a Senior Principal Medical Writer to develop regulatory documents and manage writing projects. This role involves collaboration with cross-functional teams to ensure timely delivery of quality documents. The ideal candidate will have an advanced degree in life sciences and experience with global regulatory submissions. Join us to help improve patients’ lives with innovative therapies.
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