Read from the company's own careers page; you apply on their site.
How well do you fit this job?
Upload your resume to see each requirement checked against your profile, in under a minute.
The role involves providing medical expertise for trial oversight and safety concerns, reviewing and validating protocol requirements, performing quality control checks, developing and validating SAS programs and clinical trial datasets, and ensuring compliance with applicable SOPs and quality standards.The candidate will collaborate with study teams, statistical programmers, study leads, offshore teams, and onshore/client stakeholders to ensure smooth study execution.
Amazon·Bengaluru
Emmes Group·Bengaluru
Labcorp·Bengaluru
Merck KGaA·Bengaluru