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Precision for Medicine, a global precision medicine clinical research services organization, is seeking a Clinical Data Associate II to support clinical trial data management operations. This role is based remotely and candidates can be located in Hungary, Poland, Romania, Serbia, or Slovakia.
The Clinical Data Associate II provides comprehensive data management support throughout the clinical trial lifecycle, from study startup through post-database lock. Working under direct supervision, you will support the Lead Data Manager and contribute to multiple aspects of the data management process.
Key responsibilities include: supporting the Lead DM as a backup team member; performing data entry for paper-based CRF studies; conducting quality control of data entry; developing CRF specifications from clinical study protocols; assisting in building and testing clinical databases; specifying requirements for edit checks; creating and maintaining data management documentation; training clinical research personnel on study-specific systems; reviewing and querying clinical trial data; running patient and study-level reporting; performing medical coding; assisting with SAE/AE reconciliation; liaising with third-party vendors; supporting SAS programming activities; identifying and troubleshooting operational issues; reviewing protocols and statistical analysis plans; participating in SOP development; communicating with sponsors and project teams; and presenting software demonstrations and training sessions.
Required qualifications: Bachelor's degree and/or equivalent related experience; approximately 2 years' experience as a Clinical Data Associate at a CRO, pharma, or biotech company; proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook); ability to handle diverse clinical research tasks; excellent organizational and communication skills; and professional English language proficiency (written and oral). Some travel may be required.