8.0 - 10.0 years

30 - 35 Lacs

bengaluru

Work from Office

JOB DESCRIPTION Job Title: Clinical Data Management QA Auditor Job Location: Semicon Park About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and...

Posted Date not available

Apply

QA Auditor- CTM Syngene

5.0 - 8.0 years

4 Lacs

bengaluru

Work from Office

JOB DESCRIPTION Job Title: Clinical Trial Management - QA Job Location: Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operati...

Posted Date not available

Apply

Manager, EDC Velocity Clinical Research

4.0 - 6.0 years

5 - 9 Lacs

kolkata, mumbai, new delhi

Work from Office

This position is responsible for configuring, managing, and supporting clinical research teams in data entry and validation, and ensuring adherence to regulatory and sponsor requirements. The EDC Manager will work closely with the site staff to optimize electronic data workflows and maintain data integrity. Responsibilities Duties/Responsibilities: Support clinical research site staff with accurate data entry, query resolution, and validation checks to ensure data quality. Ensure data management processes adhere to Good Clinical Practice (GCP), FDA, and sponsor-specific regulations. Monitor data discrepancies, perform data cleaning activities Work closely with clinical research teams, sponso...

Posted Date not available

Apply

Page 28 of 28

Previous 25 26 27 28

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.