ram dilip

Support clinical trial operations across multiple therapeutic areas, maintain audit-ready project documentation, and coordinate training and stakeholder communications to ensure on-time, on-budget trial execution.

Led site management and clinical operations for oncology and multi-therapeutic global trials, conducting SIVs/SMVs/SCOVs across 15 sites and ensuring protocol adherence, regulatory compliance, and data quality.

Executed monitoring and site management for oncology, infectious disease, and endocrinology studies across multiple sites, performing routine monitoring, CRF review, and regulatory audits while mentoring junior CRAs.

Managed multi-site trial operations with emphasis on regulatory coordination, TMF/ISF management, and process improvements while performing on-site and remote monitoring per study plans.

Managed operations across nine pharmacy locations, supervising staff, controlling inventory, and maintaining regulatory compliance to meet business and budget targets.

Led monitoring and quality assurance for multiple therapeutic-area trials, ensuring ICH-GCP compliance, resolving data inconsistencies, and mentoring junior clinical staff.

Completed a Project Management Certificate program with emphasis on planning, scheduling, risk management, and stakeholder communication.

Achieved SAS Certified Base Programmer for SAS 9 credential demonstrating proficiency in statistical analysis and data manipulation.

Completed a Bachelor of Pharmacy program covering pharmacology, pharmaceutics, and healthcare regulations.