Provide data management support across clinical trials from start-up to post database lock.
May perform database development and testing, and other data management activities.
Support Lead DM to ensure timely tasks and continuity.
May perform data entry for paper CRF studies and data QC.
Build and maintain clinical databases; specify edit checks and docs.
Train staff on study CRF and EDC; liaise with sponsors.

🎯 Requirements

Bachelors and/or related experience
2 to 4 years' experience
Proficiency in Microsoft Word/Excel/PowerPoint/Outlook
Able to handle a variety of clinical research tasks
Excellent organizational and communication skills
Professional use of English (written and oral)

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