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Clinical Research Associate

3+ years
Not Disclosed
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 II – Delhi, India

Job ID: JR137236
Department: Clinical Monitoring
Location: Delhi, India
Organization: ICON Strategic Solutions (Office or Home-Based)

Job Overview

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced Clinical Research Associate II to join its Strategic Solutions division in Delhi, India. This role forms a critical part of ICON’s client-dedicated programs, supporting the design, monitoring, and execution of high-quality clinical trials across therapeutic areas.

As a Clinical Research Associate II, you will contribute to the planning and oversight of clinical studies, ensure regulatory compliance, and partner with investigator sites to advance innovative medical treatments.


Key Responsibilities

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

  • Ensure adherence to study protocols, safety requirements, and ICH-GCP guidelines.

  • Maintain oversight of site performance, subject safety, and data accuracy.

  • Review source documents, verify data integrity, and resolve data queries.

  • Collaborate with investigators, coordinators, and site staff to ensure efficient study conduct.

  • Support development and review of essential study documentation such as protocols, monitoring plans, and clinical study reports.


Required Qualifications and Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare/scientific field.

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

  • Comprehensive understanding of clinical trial methodology, regulatory requirements, and ICH-GCP standards.

  • Strong communication, organizational, and documentation skills.

  • Ability to work independently while supporting cross-functional teams in a fast-paced environment.

  • Willingness to travel as required (train, car, bus, or air travel).


What ICON Offers

ICON invests in a performance-driven, diverse workforce and provides competitive compensation along with a wide range of benefits that support employee well-being and work–life balance.

Key benefits include:

  • Comprehensive annual leave programs.

  • Multiple health insurance options for employees and families.

  • Competitive retirement planning solutions.

  • Global Employee Assistance Programme (LifeWorks) with 24/7 access to wellness support.

  • Life assurance coverage.

  • Country-specific optional benefits such as childcare vouchers, gym memberships, health assessments, subsidized travel pass schemes, and more.

ICON values inclusion, accessibility, and equal opportunity. All qualified applicants are considered without bias or discrimination.


Application Process

After submitting your application, the ICON recruitment team will review your profile. Eligible candidates will be contacted with details regarding the next steps in the hiring process. Candidates requiring accommodations for medical or disability-related needs may submit a request during the application process.

If you are passionate about contributing to impactful clinical research, we encourage you to apply—even if you do not meet every listed requirement. ICON considers talent for current and future roles across the organization.