Skip to main content

Senior Document Management Associate at Novotech Global

Location
India
Type
Full-time
Level
senior
Posted

Description

The Senior Document Management Associate supports clinical research teams by managing paper and electronic Trial Master Files, uploading and tracking study documents, performing quality-control reviews, preparing TMFs for audits and regulatory inspections, and mentoring junior document management associates. The role requires more than two years of experience in a clinical research organization or equivalent role and practical experience with paper or electronic TMF activities.

For job seekers

Ready to find a role that actually fits?

Upload your résumé, start a Job Search Thread, and let Metaintro rank real openings against your experience — then guide you from search to offer.

Match

Compare live roles against your current evidence.

Position

Turn proof projects into role-specific applications.

Improve

Use market feedback to keep the skill plan current.

Return to navigation