Clinical data professional with proven track record in managing and analyzing clinical trial data. Known for reliability and adaptability in dynamic environments, with strong focus on teamwork and achieving robust results. Expertise includes data entry, management, and compliance with regulatory requirements, coupled with collaborative and results-driven approach.
Overview
1
1
year of professional experience
2
2
Languages
Work History
Clinical Data Assistant
Quintiles Research India Pvt Ltd
06.2010 - 11.2011
Perform the role of Data Entry Associate, File room Associate, Scanning Associate, Indexing Associate, or other role as defined by manager.
Process, log, and track clinical study documents in accordance with CRF Tracking and Data Entry Guidelines.
Process and enter data accurately and in a timely manner in accordance with CRF Tracking and Data Entry Guidelines.
Understand and comply with core operating procedures and working instructions.
Assist in the maintenance of Data Management Study files.
Perform CRF Tracking.
Oracle Clinical DB screen testing.
Create, review and maintain Project Specific Documents.
Create Project Specific Guidelines.
Assist in the maintenance of Data Management reports and study files.
Meet objectives as assigned.
Develop and maintain good communications and working relationships within CDM team.
Ensured accurate data entry, contributing to the successful completion of numerous clinical trials.
Maintained compliance with industry regulations and guidelines, upholding a high standard of data integrity throughout the clinical trial process.
Reduced errors in data entry through consistent attention to detail and adherence to standardized procedures.