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2.0 - 6.0 years
0 Lacs
chennai, tamil nadu
On-site
Job Description: As a Clinical Data Associate II, you will provide data management support and assistance throughout the clinical trial data management process for assigned projects under direct supervision. You will be responsible for following Standard Operating Procedures (SOPs), regulatory directives, study specific plans, and guidelines. Your duties will include supporting the Lead DM, performing data entry for paper-CRF studies, conducting quality control of data entry, developing CRF specifications, assisting in building clinical databases, maintaining quality controlled database build documentation, specifying requirements for edit check types, creating and revising data management d...
Posted 1 month ago
2.0 - 6.0 years
0 Lacs
pune, maharashtra
On-site
As a Clinical Data Associate II at our company, your role involves providing data management support and assistance throughout the clinical trial data management process for assigned projects. You will follow Standard Operating Procedures (SOPs), regulatory directives, and study-specific plans. Your responsibilities include but are not limited to: - Supporting the Lead DM as a back-up or team member to ensure continuity and timely task completion - Performing data entry for paper-CRF studies when necessary - Conducting quality control of data entry - Developing CRF specifications from the clinical study protocol and coordinating feedback - Assisting in building clinical databases - Conductin...
Posted 1 month ago
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