Looking for a job

kavya shree

@kavyashree4

I coordinate global clinical trials, streamlining study operations, data systems, vendor logistics, and project delivery.

India

Message

What I'm looking for

I'm seeking to apply my project coordination and analytical skills to support successful clinical research, compliant study delivery, and continuous process improvement.

At Clario, part of Thermo Fisher, I support clinical studies from planning and setup through monitoring and closeout. I coordinate respiratory-device vendors, study documentation, project metrics, budgets, invoicing, and client updates.

Previously at Fortrea, I built Power BI dashboards for study metrics and milestones, managed site lists and equipment tracking, and supported drug and kit shipments. I also reconciled TMF documents and system access across CTMS, Veeva eTMF, RAVE, EDC, Xcellerate, and ALMAC.

At Accenture, I supported study startup, clinical data review, Veeva Vault query management, CTMS updates, FDA Clinical Study Reports, and database-lock activities. I bring 4+ years of clinical-trial coordination experience, recognized for managing startup studies and delivering reconciled FDA appendices under tight timelines.

Experience

Work history, roles, and key accomplishments

Current

Project Coordinator

Current

Clario

Jun 2025 - Present (1 year 3 months)

Supports project management teams across all study phases, including planning, study setup, monitoring, and closeout activities. Coordinates third-party vendors, study documentation, project metrics, and financial processes while ensuring compliance with GCP and study timelines.

Project Management Clinical Trials CTMS Veeva Vault Power BI Vendor coordination Documentation Study Budgeting Invoicing Risk Tracking GCP Cross Functional Collaboration Vendor Management Issue Resolution Financial Processes

Centralized Study Associate I

Fortrea

Dec 2023 - Jun 2025 (1 year 6 months)

Maintained project directories, training matrices, and site lists while developing Power BI dashboards for study metrics. Managed document management, eTMF filing, and study system access reconciliation across multiple clinical systems.

Power BI Spotfire CTMS Veeva Vault ETMF Rave EDC Xcellerate Almac Document Management training coordination Data Analysis Clinical Trials Training Management

Clinical Data Management Associate

Accenture

Aug 2022 - Dec 2023 (1 year 4 months)

Assisted in study startup activities by creating studies in RAVE, Veeva, Eclipse, and CTMS. Reviewed clinical trial data, managed discrepancies, and prepared Clinical Study Reports for FDA submission.