Provide data management support from study start-up to post database lock.
Follow SOPs/WIs, regulatory directives, and study-specific plans.
May perform database development and testing, and other data management activities.
Back-up to Lead DM to ensure continuity and timely task completion.
May perform data entry for paper-CRF studies as needed.
Conduct database build UAT and maintain quality-controlled documentation.

🎯 Requirements

Bachelor's degree and/or related experience.
About 2 years CDA experience in CRO/Pharma/Biotech.
Proficiency in Microsoft Office: 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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