Clinical Research Associate

Aithent

1 - 5 years

1 - 5 Lacs

chennai

Posted:1 day ago| Platform:

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Skills Required

clinical research ich-gcp cra crc gcp crf clinical trials clinical data ich

Work Mode

Work from Office

Job Type

Full Time

Job Description

Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPs
Prepare and maintain documents related to clinical trials.
Generate data entry queries and test clinical applications for numerous clinical trials.
Analyze clinical trials data and prepared reports for Data Coordinator and Sponsor.
Serve as liaison between Data Management and other departments in Clinical application developments.
Manage clinical research data for the new and ongoing electronic clinical trials. Conduct UAT Testing and validate software application processes for the management of clinical trials.
Assist with the creation of data manuals for specified clinical trials.
Checked data for clinical trials and raised queries with any inaccuracies. Be responsible for the data management of specific clinical studies.
Review and maintain data management documentation, record management systems and identify tracking tools. Ensure the accuracy and integrity of data entered in eCRF.
Prepare reports and organize presentations or meetings about clinical trial progress

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