Ref #: 25634

Employment type: Permanent - Full-Time

Location: Poland

Posted: 29-Jan-2021


We are looking for passionate people who would like to join our new Data Management FSP. DOCS Global, an FSP Division of ICON Clinical, is working with a Global Biopharmaceutical company in building a large FSP team within Clinical Data Management Operations.

The Associate Study Data Manager is responsible for routine data management activities during the course of a study under the supervision of study data manager, such as data review, validation, cleaning and tracking, as well as maintaining data management documents if needed.

Please contact Dariusz Sternlicht, Recruitment Consultant at DOCS on +48 606 130 397 or email your up-to-date CV to:

Minimum of a Bachelor of Science degree in a health related field
Previous experience in a data review/data management role - 2 years preferred
Experience preferred in clinical data listing review, query generation and the use of data review tools
Demonstrated success in working independently
Strong communication

- Database Set-Up – draft CCI, Data Validation Specifications, Reports Specifications, external data transfer specifications etc., facilitate the documents review, set up peripheral tools, and perform AT/UAT
- Centralized Monitoring Plan – support preparation, review and update
- Data Validation and Review – perform routine DM activities according to Centralized Monitoring Plan, provide DM status reports, monitor data validation throughout study lifecycle
- CRF – support CRF revision if needed
- Database Lock – support the SDM in implementation of the procedures prior to DBL including technical issue resolution
- Quality – perform quality checks and put in place CAPA if needed