Study Delivery Sr Associate in Hyderabad, India - Jobeax
Vacancy description
Study Delivery Sr Associate in Hyderabad, भारत
Amgen
Hyderabad, भारत
Senior Associate providing study management support to clinical research teams at Amgen in Hyderabad. Responsible for coordinating study planning, monitoring execution, managing vendors and systems, and ensuring regulatory compliance throughout the trial lifecycle.
Responsibilities
Develop and maintain study trackers, dashboards, timelines, and tools for vendor and supply management
Monitor global enrollment, data flow, and quality indicators; proactively address deviations and risks
Coordinate investigator meetings, trial events, site communications, and start-up activities
Manage clinical trial documentation and systems; ensure accurate data entry and inspection readiness
Support recruitment strategies, training oversight, vendor setup, and escalate issues to stakeholders
Requirements
Master's degree OR Bachelor's with 2+ years clinical execution experience OR Associate's with 6+ years OR High school diploma with 8+ years
3 years life sciences work experience including 1 year biopharmaceutical clinical research at biotech, pharma, or CRO
Experience with global clinical trials and clinical trial management systems (CTMS, eTMF, EDC)
Strong proficiency in MS Office (Word, Excel, PowerPoint) and data management tools
Knowledge of risk-based monitoring, audit processes, CAPA implementation, and regulatory compliance
Vendor oversight and supplier management experience
Demonstrated collaborative communication, attention to accuracy, and problem-solving abilities
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