Opening for Clinical Data Associate @ Novo Nordisk
-About the Department
GD-GSC-Data Management Unit supports Projects and Trial Management on operational Data Management activities of clinical projects. The key objective of the department is to ensure high quality data delivery to the stakeholders. The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout. The major activities handled include CRF Design, Database set-up & Programming, Data Entry, Data Validation, Medical Coding, Lab data handling, Data analysis & migration, Database Lock, Hyperlinking and Bookmarking and Project Management. These opportunities have in turn fostered a deeper understanding with an ability to drive, contribute to process and share best practices while leveraging cross-cultural collaboration towards a unified mission to achieve clean data.
-The Job
Clinical Data Associate is responsible for below mentioned activities
Data entry of clinical trial data into database with accuracy and speed.
Ensuring the integrity of clinical trial databases
Accountability and tracking of documents for each batch received and report any discrepancies to trial data manager.
Scanning, filing, cleaning of CRFs and other documents as per project requirements.
Involve in archiving of Trial related documents to HQ or locally as per TMFArchive specification.
Qualifications
Batchelor's degree in Life Science.
Data entry experience; preferably on clinical database systems.
Computer literacy: Proficient in Microsoft Office tools.
Employment Type: Contract Position
Deadline: 3 July 2015
At Novo Nordisk, decisions and actions are based on their positive impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.
Click here to apply
-About the Department
GD-GSC-Data Management Unit supports Projects and Trial Management on operational Data Management activities of clinical projects. The key objective of the department is to ensure high quality data delivery to the stakeholders. The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout. The major activities handled include CRF Design, Database set-up & Programming, Data Entry, Data Validation, Medical Coding, Lab data handling, Data analysis & migration, Database Lock, Hyperlinking and Bookmarking and Project Management. These opportunities have in turn fostered a deeper understanding with an ability to drive, contribute to process and share best practices while leveraging cross-cultural collaboration towards a unified mission to achieve clean data.
-The Job
Clinical Data Associate is responsible for below mentioned activities
Data entry of clinical trial data into database with accuracy and speed.
Ensuring the integrity of clinical trial databases
Accountability and tracking of documents for each batch received and report any discrepancies to trial data manager.
Scanning, filing, cleaning of CRFs and other documents as per project requirements.
Involve in archiving of Trial related documents to HQ or locally as per TMFArchive specification.
Qualifications
Batchelor's degree in Life Science.
Data entry experience; preferably on clinical database systems.
Computer literacy: Proficient in Microsoft Office tools.
Employment Type: Contract Position
Deadline: 3 July 2015
At Novo Nordisk, decisions and actions are based on their positive impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.
Click here to apply
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