Associate Study Data Manager - home- based
- Company
- Docs Global (Continental Europe)
- Location
- Poland
- Salary
- Competitive
- Posted
- 03 Feb 2021
- Closes
- 04 Mar 2021
- Ref
- 25634
- Discipline
- Clinical Research, Clinical Study Manager
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
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
#datamanagementjob
#DMjob
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
#datamanagementjob
#DMjob