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2.0 - 6.0 years
0 Lacs
hyderabad, telangana
On-site
You will be supporting the Study Lead in TCO studies to ensure all trial deliverables are met according to timelines, budget, operational procedures, and quality standards. Your role will involve assisting TCO CSD, CSaD, and CSTL in the development of study documents, tools, guidelines, and training materials. You will also be responsible for managing clinical study material and implementing issue resolution plans. Under the supervision of CSD, CSaD, and CSTL, you will play a key role in preparing CSR appendices. Additionally, you will be setting up and maintaining appropriate study tracking forms, including enrollment logs, site and vendor contact lists, drug shipping logs, and team members...
Posted 3 months ago
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