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Clinical Research Associate

2+ 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

 

Clinical Research Associate – Remote | Chennai & New Delhi


Meta Title: Clinical Research Associate – Remote India

Meta Description: Hiring CRA in Chennai & New Delhi. Remote clinical trials job with ICON. Apply now to join global pharma leaders in oncology research.

Meta Keywords: clinical research associate jobs India, CRA Chennai Delhi, oncology clinical trials jobs, remote CRA role, ICH-GCP jobs, ICON careers India


Job Summary

ICON plc, the world’s largest healthcare intelligence and clinical research organization, is hiring a Clinical Research Associate (CRA) for a remote position based in Chennai and New Delhi. This is a client-embedded opportunity offering involvement in oncology clinical trials and global monitoring practices. If you're passionate about advancing healthcare and contributing to life-saving research, this role offers the ideal combination of remote flexibility and impactful clinical work.


Key Responsibilities

  • Manage the full lifecycle of clinical trial sites from site selection through to close-out

  • Conduct on-site monitoring visits, ensuring adherence to study protocols and ICH-GCP guidelines

  • Maintain high-quality data through diligent site management and monitoring

  • Collaborate with the client’s study team while being supported by an ICON line manager

  • Ensure regulatory compliance and quality assurance standards

  • Support and mentor other CRAs or junior team members when needed


Required Skills & Qualifications

  • Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm/Pharm D), Dentistry (BDS), or Medicine (MBBS)

  • Minimum 2 years of independent on-site monitoring experience in oncology studies (excluding induction/training)

  • In-depth understanding of ICH-GCP and local Indian regulatory frameworks

  • Excellent written and verbal communication skills

  • Residing in or willing to travel within Chennai or New Delhi

  • Ability to manage remote work with minimal supervision


Perks & Benefits

  • Competitive salary (exact range not specified)

  • Work-from-home flexibility with field-based monitoring

  • Structured career development programs

  • Access to a global Employee Assistance Programme (TELUS Health)

  • Comprehensive health insurance for you and your family

  • Retirement savings and life assurance options

  • Additional country-specific perks such as gym discounts, childcare vouchers, and subsidized travel


Company Overview

ICON plc is a global leader in clinical research, providing outsourced development and commercial services to pharmaceutical, biotechnology, and medical device companies. With a mission to accelerate the development of drugs and devices that save lives, ICON delivers operational excellence in complex clinical trials across more than 90 countries.


Work Mode

Remote (Home-based) – Candidates must be located in or near Chennai or New Delhi


Call to Action

Ready to take your clinical research career to the next level in a meaningful oncology program?
Apply now and become part of a global CRO that's driving innovation in life sciences.

Visit ICON Careers for more details on our culture and employee benefits.