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Cra I /Ii

ICON
3+ years
Not Disclosed
Mumbai, India
1 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Clinical Research Associate I / II (CRA I / II)

Job Title: Clinical Research Associate I / II (CRA I / II)
Location: Mumbai, India
Work Model: Office With Flex
Employment Type: Full-Time
Job Requisition ID: JR135624
Company: ICON plc


About ICON

ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of innovative medicines and therapies that improve patient lives worldwide.

Guided by its core values of Integrity, Collaboration, Agility, and Inclusion, ICON fosters a culture of excellence, innovation, and continuous learning across its global workforce.


Position Overview

ICON is seeking an experienced Clinical Research Associate (CRA I / II) to join its Clinical Operations team. In this role, you will be responsible for the successful execution and monitoring of clinical trials, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

The position requires strong site management expertise, extensive monitoring experience, and therapeutic area knowledge in Oncology and/or Immunology.


Key Responsibilities

Site Management & Monitoring

  • Conduct Site Qualification Visits (SQV), Site Initiation Visits (SIV), Monitoring Visits (MV), and Close-Out Visits (COV).

  • Evaluate site readiness and ensure study requirements are understood and implemented.

  • Monitor study progress and site performance throughout the clinical trial lifecycle.

  • Verify source documentation and ensure accurate data collection.

Clinical Trial Oversight

  • Ensure compliance with:

    • Study protocols

    • ICH-GCP guidelines

    • Sponsor requirements

    • Regulatory requirements

    • Ethical standards

  • Identify protocol deviations and support corrective and preventive actions.

  • Monitor patient safety and study conduct at investigative sites.

Data Quality & Compliance

  • Perform source data verification (SDV).

  • Review clinical data for accuracy, completeness, and consistency.

  • Manage and resolve data queries in a timely manner.

  • Ensure data integrity throughout the study.

Site Relationship Management

  • Build and maintain effective relationships with investigators, study coordinators, and site personnel.

  • Provide ongoing site training and support.

  • Act as the primary liaison between investigative sites and study teams.

Study Documentation & Reporting

  • Prepare detailed monitoring reports and follow-up letters.

  • Contribute to the review and maintenance of:

    • Clinical study protocols

    • Study plans

    • Clinical study reports

    • Trial master file documentation

  • Ensure documentation is inspection and audit ready.


Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Nursing

    • Biotechnology

    • Medical Sciences

    • Other Healthcare or Scientific Discipline


Experience

  • Minimum 3 years of Clinical Research Associate experience.

  • Strong on-site monitoring experience is mandatory.

  • Experience conducting independent monitoring visits across multiple sites.

  • Proven ability to manage clinical trial activities from initiation through closeout.