Ref #: 25634

Employment type: Permanent - Full-Time

Location: Poland

Posted: 29-Jan-2021

Description

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.

HOW TO APPLY:
Please contact Dariusz Sternlicht, Recruitment Consultant at DOCS on +48 606 130 397 or email your up-to-date CV to: dariusz.sternlicht@docsglobal.com


REQUIREMENTS:
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


KEY RESPONSIBILITIES:
- 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

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