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Job Location | Bangalore |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | IT - Software |
Functional Area | Sales / BD,General / Other Software |
EmploymentType | Full-time |
About the position:
The Clinical Document Management Associate (CDMA) will provide support for Trial Master File (TMF) activities to the clinical teams. This role will be responsible for working with study teams, both internal and external, to manage Trial Master Files (TMF), both electronic and paper in format according to project requirements, ICH GCP guidelines local/global regulatory requirements and Novotech/Client SOPs.
Core responsibilities:
Required Qualification(s):
Keyskills :
salesmanagementmarketingbillingdrivingmusic makingquality controlclinical trialsmonthly reportsspecial projectsclinical researchdocument managementclinical operationshealthcare industryclinical developmentregulatory requirementspharmaceuti