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Cra Ii

3+ years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Meta Title

CRA II Job in Mumbai or Pune | ICON Clinical Research

Meta Description

Apply for CRA II at ICON in Mumbai or Pune. Join oncology trials, phase II–IV studies. Competitive benefits and a dynamic clinical research environment.

Meta Keywords

CRA II jobs Mumbai, Clinical Research Associate India, ICON careers India, oncology clinical trials, ICH-GCP jobs, phase 2 and 3 trials, clinical research monitoring jobs, pharma jobs Mumbai, clinical operations Pune


Clinical Research Associate II (CRA II) – Mumbai or Pune | ICON plc

Job Summary

ICON plc, a global leader in clinical research and healthcare intelligence, is seeking a Clinical Research Associate II (CRA II) to join its growing operations in Mumbai or Pune. In this role, you will independently manage and monitor investigational sites participating in phase II–IV clinical studies, with a particular focus on oncology trials. This position offers a chance to work within an established, innovative CRO environment committed to improving patient outcomes worldwide.


Key Responsibilities

  • Independently conduct site qualification, initiation, monitoring, and close-out visits

  • Ensure regulatory and protocol compliance, including adherence to ICH-GCP

  • Manage ethics and IRB submissions for protocols and informed consent forms

  • Handle sponsor-generated queries and ensure timely resolution

  • Monitor study progress and ensure data quality, patient safety, and compliance

  • Support preparation of study documents and feasibility evaluations for new proposals

  • Participate in mentoring and training junior clinical research associates


Required Skills and Qualifications

  • Minimum 3 years of experience monitoring phase I–III clinical trials

  • Bachelor’s degree or equivalent in Medicine, Life Sciences, or a related discipline

  • Hands-on experience in Oncology clinical trials preferred

  • Strong knowledge of ICH-GCP guidelines and regulatory compliance

  • Excellent written and verbal communication skills

  • Willingness to travel at least 60%, including both domestic and international travel

  • Valid driver's license required


Perks and Benefits

  • Competitive salary (not publicly disclosed)

  • Multiple annual leave entitlements

  • Comprehensive health insurance options for you and your dependents

  • Competitive retirement planning and savings plans

  • Global Employee Assistance Programme (TELUS Health)

  • Life assurance

  • Flexible, location-specific benefits including discounted gym memberships, childcare vouchers, and more


Company Description

ICON plc is a leading global clinical research organization (CRO) delivering clinical development solutions and healthcare intelligence across pharmaceutical, biotech, and medical device industries. ICON is recognized for driving innovation, maintaining quality, and creating impactful outcomes in global clinical research.


Work Mode

On-site with travel from Mumbai or Pune


Call to Action

If you are an experienced CRA looking to elevate your clinical research career in oncology and global studies, this is your opportunity. Join ICON’s expert team and be part of research that transforms lives. Apply now and advance your future in clinical trials with a world-class CRO.