Aarthy Chandru

Clinical Research | Regulatory Compliance | Proud Deaf Woman

Role
Regulatory Compliance-human Subject Protection Program at Valley Health System
Location
New Providence, NJ, US
LinkedIn followers
500 followers
Healthcare & Human ServicesView LinkedIn profile

About Aarthy Chandru

Experienced Clinical Research Professional with a strong background in managing clinical trials, regulatory compliance, and digital health studies. Proven expertise in leading complex projects, collaborating with cross-functional teams, and ensuring adherence to GCP, FDA, and IRB guidelines. Skilled in utilizing various CTMS, EDC, and EMR systems to streamline operations and improve trial efficiency. Dedicated to advancing clinical research through innovative approaches in digital health and patient-centered care

Experience

  1. Regulatory Compliance-human Subject Protection Program

    Valley Health System

    Oct 2024 — Present · Paramus, NJ, US

    Responsible for overseeing three key areas within Valley\'s Research Department: Regulatory Compliance, Accreditation and Education for research programs, and Corporate Compliance.

Education

  • Harvard Medical School

    Global Clinical Scholar Research Training ( GCSRT), Medical Clinical Sciences/Graduate Medical Studies

  • Rutgers University

    Master of Science (MS), Clinical Trials Sciences

    2012 — 2014

  • Anna University Chennai

    Bachelor of Technology (B.Tech.), Pharmaceutical Sciences

    2006 — 2010

Skills

  • Ich-Gcp
  • Clinical Monitoring
  • Clinical Trial Management System (Ctms)
  • Life Sciences
  • Clinical Research
  • Tmf
  • Argus Safety
  • Regulatory Affairs
  • Irb
  • Pharmacovigilance

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Aarthy Chandru — Regulatory Compliance-human Subject Protection Program at Valley Health System in New Providence, NJ, US | Unifers