Document Management Associate at Novotech Global
Bangalore, karnataka, India -
Full Time


Start Date

Immediate

Expiry Date

29 Jun, 26

Salary

0.0

Posted On

31 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Trial Master File (TMF), Electronic TMF (eTMF), Paper TMF Management, ICH GCP Guidelines, Regulatory Requirements, SOP Compliance

Industry

Biotechnology Research

Description
DOCUMENT MANAGEMENT ASSOCIATE (DMA) The Document Management Associate (DMA) 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.
Responsibilities
The Document Management Associate will support clinical teams by managing both electronic and paper Trial Master Files (TMF) according to project requirements and regulatory guidelines. This involves working with internal and external study teams to ensure proper file maintenance.
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