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Cra I /Ii

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ICON
3 years
Not Disclosed
Mumbai, India
10 Feb. 27, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Associate (CRA I / II) – Mumbai, India

Location: Mumbai, India
Work Model: Office-Based with Flexible Options
Job Type: Full-Time
Job Requisition ID: JR135624
Industry: Clinical Research / Pharmaceuticals

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced Clinical Research Associate (CRA I / II) to join our Mumbai team. This role is ideal for professionals with a strong background in oncology or immunology clinical trials who are committed to ensuring data integrity, protocol compliance, and patient safety.

Role Overview

As a CRA I / II at ICON, you will be responsible for monitoring clinical trial sites, conducting on-site visits, reviewing data, and supporting the preparation of clinical documentation. You will play a critical role in advancing clinical studies and ensuring the delivery of high-quality data in alignment with ICH-GCP and regulatory guidelines.

Key Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits for assigned clinical trials.

  • Ensure strict adherence to study protocols, data integrity, and patient safety requirements.

  • Collaborate with investigators and site staff to facilitate smooth and efficient study execution.

  • Review clinical data and resolve queries to maintain high-quality datasets.

  • Assist in the preparation, review, and maintenance of study documentation, including protocols and clinical study reports.

  • Identify and escalate potential risks, deviations, or compliance issues to project management as appropriate.

Required Experience & Skills

  • Bachelor’s degree in a scientific or healthcare-related field.

  • Minimum 3 years of experience as a Clinical Research Associate with on-site monitoring responsibilities.

  • In-depth knowledge of clinical trial operations, ICH-GCP guidelines, and regulatory requirements.

  • Mandatory experience in Oncology or Immunology therapeutic areas.

  • Strong organizational, analytical, and communication skills with excellent attention to detail.

  • Ability to work independently and collaboratively in a fast-paced, dynamic environment.

  • Willingness to travel up to 60% internationally and domestically (fly and drive) with a valid driver’s license.

What ICON Offers

  • Competitive salary with global career growth opportunities.

  • Comprehensive benefits including health insurance, retirement planning, life assurance, and wellness programs.

  • Professional development, training, and mentorship programs to advance your career.

  • Inclusive and diverse workplace culture that values innovation, collaboration, and operational excellence.

  • Employee assistance programs and work-life balance support to ensure personal and professional well-being.

ICON is committed to an inclusive and accessible workplace free from discrimination. All qualified applicants will receive equal consideration regardless of race, gender, religion, disability, or other protected status.

This role is ideal for CRAs seeking to contribute to impactful oncology or immunology trials while advancing their clinical research career in a global organization. Apply now to join ICON’s Mumbai team.