Posted:3 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities Ensure compliance with ICH-GCP guidelines and regulatory requirements. Collaborate with cross-functional teams to develop study protocols and reports. Analyze data, identify trends, and draw conclusions from experiments. Maintain accurate records of patient information, test results, and trial outcomes Supervision of planning , scheduling & execution of BA / BE studies for timely commencement , conduct & conclusion of the projects. Responsible for ensuring that the study is conducted in compliance with the protocol , Good Clinical Practice , guidelines , regulatory & ethical principles. Preferred candidate profile Post MD with ,minimum 1 year experience Candidates with 15days - 30 days notice period preferred. Email : monisha.lahiri@randstad.in
Randstad
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