Ancy Feona

Initiation Clinical Research Associate I at Parexel | Clinical Research & Study Start-Up | Regulatory Affairs | EU CTIS & CTA Submissions | Veeva Vault | Global Clinical Trials | Ex-IQVIA | Ex-Pfizer

Role
Initiation Clinical Research Associate i at Parexel
Location
Bengaluru, KA, IN
LinkedIn followers
500 followers
Healthcare & Human ServicesView LinkedIn profile

About Ancy Feona

Clinical Research professional with ~4 years of experience in Regulatory Affairs and global clinical trial support. Currently working as an Initiation Clinical Research Associate I at Parexel, supporting study start-up activities including Clinical Trial Applications (CTA), EU CTIS coordination, regulatory submissions, and essential document review. Previously worked at IQVIA as a Clinical Regulatory Services Lead supporting US and EU regulatory projects, and earlier contributed to regulatory publishing and product license support for Pfizer. Experienced in global clinical trial operations, site regulatory documentation, and cross-functional collaboration to ensure regulatory compliance. Skilled in systems such as Veeva Vault, CTIS, eTMF, and CTMS. Passionate about supporting efficient study start-up and successful execution of global clinical trials.

Experience

  1. Initiation Clinical Research Associate i

    Parexel

    Mar 2026 — Present · Bengaluru, IN

Education

  • St. Joseph's college Trichy

    Masters, General chemistry

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Ancy Feona — Initiation Clinical Research Associate i at Parexel in Bengaluru, KA, IN | Unifers