Srini Vasan

Experience

1. Site Activation - Due Diligence Specialist i

   ICON plc

   Sep 2024 — Present · Chennai, IN

   Conduct comprehensive due diligence compliance searches for investigator sites prior to CDP approval.Maintain and update the ICON Investigator Database with FOI Check/World Check outcomes and team feedback.Approve and verify site and PI (Principal Investigator) regulatory compliance to enable clinical trial progression.Ensure alignment with FDA, CFDA, EMA, and other local/international regulatory board standards.Perform detailed World Check screenings to identify discrepancies in investigator and institutional data.Coordinate with the Legal Compliance team to resolve regulatory flags or historical issues.Conduct medical license verifications for investigators and validate against local medical councils and databases.Review clinical reporting documents, support audit readiness, and collaborate on internal/external audits.Run customized compliance reports and support escalations, ensuring timely communication with internal stakeholders and clients.Actively contribute to improving internal workflows and risk assessment protocols related to site selection.Liaise with cross-functional teams including regulatory, legal, and medical writing to ensure audit trail transparency.Foster effective sponsor and client relationships by delivering high-standard responses and proactive compliance support.

Education

• Erode cancer centre

  Clinical research intern

• I.R.T. PERUNDURAI MEDICAL COLLEGE & RESEARCH CENTRE (Inst. Code - 013), ERODE

  Clinical pharmacist intern

• NANDHA COLLEGE OF PHARMACY (Inst. Code - 051), ERODE

  Doctor of Pharmacy - PharmD, Pharmaceutical Marketing and Management

  2017 — 2023