Diploma or a 1-year course in Clinical Research is
mandatory
, along with relevant working experience.
Job Location:
Prabhadevi, Mumbai, Maharashtra - 400025
Responsibilities:
Obtain screening and informed consent from volunteers
Record demographics, study logs, and self-evaluation
Fill out habit questionnaires and other relevant forms
Address volunteer queries and ensure smooth study flow
Maintain study-related relevant documents
Handle data entry, verification, and quality checks of documents
Operate instruments and ensure study-related documentation is complete
Archive study-related records and maintain compliance
Prepare study-related documents including
protocols, reports, and study logs
Assist in
study design, protocol development, and ethical submissions
Coordinate with investigators, project teams, and sponsors for study updates
Review and ensure
accuracy of Case Report Forms (CRFs)
and other study documents
Conduct periodic
site monitoring, audits, and ensure protocol adherence
Train junior CRAs and study team on protocol requirements and GCP compliance
Job Types: Full-time, Permanent
Pay: ?23,468.95 - ?40,000.00 per month
Benefits:
Food provided
Health insurance
Leave encashment
Paid sick time
Paid time off
Provident Fund
Schedule:
Day shift
Fixed shift
Monday to Friday
Application Question(s):
Have you worked in Cosmetic Clinical Trials?
Experience:
Clinical research Associate: 3 years (Required)
Work Location: In person
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