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Senior Global Trial Associate
On-site · Hyderabad, Telangana, India
Job Summary
Senior Global Trial Associate responsible for support of Global Trial Lead in planning, execution, and oversight of multiple clinical studies across varying stages. Primary focus on operational delivery including eTMF accuracy, development and collection of study-level documentation, vendor management, country regulatory approvals/notifications, CTMS milestones, and cross-functional collaboration. Roles include proactive risk identification, escalation, study meetings leadership, and contribution to study closure/archival activities. Requires knowledge of ICH/GCP, regulatory guidelines, and the drug development process; BA/BS and 2-4 years’ clinical research experience with global exposure preferred. The role encompasses working with cross-functional teams to drive study execution and ensure deliverables meet timelines and budget constraints.
Required Qualifications
- BA/BS in relevant discipline strongly preferred
- Minimum 2-4 years’ experience in Clinical Research or related work experience
- Global experience is preferred
- Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems
- Travel required less than 5%
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