Provide data management support from study start-up to database lock.
Follow SOPs/WIs and regulatory directives across projects.
Perform database development and testing, plus other data management activities.
Back-up support for Lead DM to ensure continuity and timely task completion.
May perform data entry for paper-CRF studies, as needed.
May perform quality control of data entry.

🎯 Requirements

Bachelors and/or a combination of related experience
Around 2 years\' experience as a Clinical Data Associate in a 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 the English language; both written and oral

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