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Full-Time
Salary: 25k to 30k
Positions: 10

Pharmacovigilance Services Associate

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Job Description

Location: Bangalore, India
Job ID: JR137944
Company: ICON plc
Department: Clinical Monitoring — ICON Strategic Solutions
Work Model: Remote / Field-based

Job Overview

ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to shaping the future of clinical development. As a Clinical Research Associate 1 (CRA 1), you will play a vital role in managing, monitoring, and coordinating clinical trials while ensuring adherence to regulatory standards, patient safety, and data integrity.

This position offers an opportunity to work in a collaborative, innovation-driven environment that fosters professional growth and values diversity and inclusion.

Role & Responsibilities

  • Coordinate all start-up and monitoring activities for clinical studies, ensuring compliance with study protocols and regulatory guidelines.
  • Complete study status reports accurately and maintain thorough documentation of all study-related activities.
  • Manage and resolve sponsor-generated queries efficiently to support study progress.
  • Participate in study feasibility assessments and contribute to the preparation and review of study documentation.
  • Build and maintain collaborative relationships with investigators, site staff, and other key stakeholders.
  • Ensure patient safety and data quality through adherence to ICON’s SOPs, ICH-GCP guidelines, and regulatory requirements.
  • Support the team in achieving cost efficiency and timely delivery of study milestones.

Educational Qualification

  • Education: University degree in Medicine, Life Sciences, or equivalent discipline.
  • Experience: 1–4 years of experience in onsite monitoring.
  • Knowledge: Strong understanding of ICH-GCP guidelines and ability to interpret medical data.

Location

 Bangalore, India

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