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0.0 years
0 Lacs
bengaluru, karnataka, india
On-site
Accountabilities For This Role Include Accountable for study start-up and the maintenance of regulatory and ethics committee (EC) submissions, overseeing the collection, preparation, review, and tracking of documents required for the application process. Where applicable, responsible for submitting the appropriate applications and documentation to Regulatory Authorities and/or IEC/IRB during the start-up period, liaising with regulatory bodies and ethics committees and ensuring expertise in the regulatory field. Actively participate in Local Study Team (LST) meetings. In some countries, these activities may be performed by the regulatory department. Ensure timely updating of Clinical Trial M...
Posted 1 month ago
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