Principal Medical Writer
GSK
full-time
Posted on:
Location Type: Office
Location: Bengaluru • 🇮🇳 India
Visit company websiteJob Level
Lead
Tech Stack
Google Cloud Platform
About the role
- Drive and coordinate the process to draft, review and approve written assignments.
- Work in a matrix team to ensure delivery of high quality clinical documents.
- Proven track record in writing clinical regulatory documents.
- Ability to quickly assess complex situations and implement effective plans for solutions.
- Familiarity with approaches to expedite document preparation.
Requirements
- PhD or relevant working experience within the life sciences space.
- Clinical regulatory writing experience in the pharmaceutical industry
- Demonstration of leadership.
- Experience in multicultural settings.
- Ability to interpret, describe and document clinical data.
- Working knowledge of International Committee for Harmonisation (ICH)/Good Clinical Practice (GCP).
- Computer skills and general computer literacy.
- Excellent English language skills (verbal and written).
Benefits
- Not specified 📊 Resume Score Upload your resume to see if it passes auto-rejection tools used by recruiters Check Resume Score
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical regulatory writingdocument preparationclinical data interpretationwriting clinical documents
Soft skills
leadershipproblem-solvingcommunicationcollaboration
Certifications
PhD