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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

 

Meta Title

Clinical Research Associate Job - Chennai & Delhi | ICON

Meta Description

Hiring Clinical Research Associate for oncology trials in Chennai & Delhi. Remote role with ICON. 2+ years onsite monitoring experience required.

Meta Keywords

clinical research associate jobs, CRA oncology jobs, clinical monitoring jobs India, ICON clinical research associate, remote CRA jobs Chennai, clinical trial monitoring Delhi, pharma jobs India


Clinical Research Associate - Oncology | ICON - Remote (Chennai & Delhi)

Location: Chennai, Delhi
Employment Type: Full-Time
Work Mode: Remote (Home-based) with local presence in Chennai or Delhi


Job Summary

Join ICON, the world’s largest clinical research organization, as a Clinical Research Associate (CRA) specializing in oncology. This remote role, based in Chennai or Delhi, offers the opportunity to perform end-to-end clinical trial monitoring, ensuring data quality and regulatory compliance. The position involves active site management, collaboration with study teams, and mentoring responsibilities, making it ideal for professionals with 2+ years of oncology monitoring experience seeking growth in clinical research.


Responsibilities

  • Manage all CRA duties including site selection, initiation, routine monitoring visits, close-out, and database lock

  • Ensure high-quality clinical trial data with low query rates and positive Quality Assurance reports

  • Collaborate closely with clients’ study teams and ICON line managers for smooth study conduct

  • Support, train, and mentor junior CRA team members to enhance overall team performance

  • Oversee compliance with clinical trial protocols and regulatory guidelines during site monitoring


Required Skills & Qualifications

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

  • Minimum 2 years of onsite oncology clinical trial monitoring experience (excluding training/induction)

  • Strong verbal and written communication skills for effective coordination with study teams and sites

  • In-depth knowledge of clinical trial monitoring, GCP, and regulatory compliance

  • Ability to work remotely while maintaining effective local presence in Chennai or Delhi


Perks & Benefits

  • Work remotely with support from ICON’s global clinical research infrastructure

  • Opportunity to work with the largest clinical research organization in the world

  • Exposure to oncology clinical trials and career development opportunities

  • Inclusive and empowering work culture that values innovation and continuous improvement

  • Supportive management and structured mentoring programs


Company Description

ICON plc is a leading global clinical research organization specializing in healthcare intelligence and clinical trial management. We deliver innovative, data-driven solutions to pharmaceutical, biotech, and medical device companies worldwide, driving the future of clinical development.


Work Mode

Remote (Home-based) with location requirement in Chennai or Delhi


Call to Action

Are you a dedicated Clinical Research Associate with oncology monitoring experience? Apply now at ThePharmaDaily.com to join ICON’s innovative team and contribute to advancing lifesaving clinical research.