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| Job Location | Chennai |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Recruitment Services |
| Functional Area | Medical Transcription |
| EmploymentType | Full-time |
* Graduate background (e.g. Bachelors degree) in scientific field plus some professional experience in a clinical research- related position (two years in Clinical Development or equivalent). * Non-graduate jobholders require a substantial amount of professional experience in a clinical research related position (minimum of 2 years) and additional qualifications that also provide exposure to fundamental clinical research related skills & knowledge * Good oral and written communication in English * Familiar with Trial Master File Handling, including use of eTMF System * Familiar with use of CTMS System * Ability to work in an international/ multicultural cross functional matrix environment * Good understanding of the policies and procedures of Clinical Operations and of ICH-GCP * Good administrative, coordination and problem- solving skills * Good time and priority management, ability to work efficiently under pressure * Strong computer skills including knowledge of MS Office (Excel , Word , PowerPoint ), Outlook and TEAMS skillsclinical trails,
Keyskills :
clinical researchclinical trialsdata collectionaccountabilityannual reportsms officecomputer skillsclinical operationsclinical developmentwritten communication