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Clinical Research Associate

3 years
Not Disclosed
10 Dec. 5, 2025
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 II – Delhi

Location: Delhi, India
Job ID: JR137236
Department: Clinical Monitoring | ICON Strategic Solutions
Work Model: Office or Home Based

About the Role

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Clinical Research Associate II to join its Strategic Solutions (FSP/Client Dedicated Program) team in Delhi. This position plays a critical role in the monitoring and execution of clinical trials, ensuring high standards of data quality, regulatory compliance, and patient safety.

This role is suited for experienced CRAs who thrive in collaborative environments, maintain high attention to detail, and are committed to advancing clinical development through operational excellence.


Key Responsibilities

  • Conduct site qualification, initiation, routine monitoring, and close-out visits in accordance with study protocols and regulatory expectations.

  • Ensure ongoing compliance with ICH-GCP guidelines, trial protocols, and applicable regulatory requirements.

  • Maintain high-quality clinical data through proactive data review, issue identification, and timely resolution of queries.

  • Collaborate effectively with investigators, coordinators, and site personnel to support efficient study conduct and patient safety.

  • Review and contribute to study-related documents, including protocols, monitoring plans, and clinical study reports.

  • Provide ongoing updates and risk-based insights to project teams to ensure study goals are met.


Qualifications & Experience Requirements

  • Bachelor’s degree in life sciences, pharmacy, nursing, or a related scientific discipline.

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

  • Strong understanding of clinical trial processes, regulatory frameworks, and ICH-GCP requirements.

  • Excellent organizational, communication, and documentation skills with strong attention to detail.

  • Ability to work independently while contributing effectively within cross-functional teams.

  • Willingness and ability to travel via train, car, bus, or air as required for site visits.


What ICON Can Offer You

ICON is committed to fostering a diverse, high-performing work culture that values professional growth and supports employee well-being.

Sample Benefits Include:

  • Competitive annual leave

  • Comprehensive health insurance options

  • Retirement planning benefits

  • Global Employee Assistance Programme (LifeWorks)

  • Life assurance coverage

  • Flexible, country-specific optional benefits such as childcare vouchers, gym memberships, travel subsidies, and more

For full details, visit the ICON careers site.


Commitment to Inclusion

ICON is dedicated to providing an inclusive and equitable workplace. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Candidates requiring reasonable accommodation due to medical conditions or disabilities may submit a request through the designated process.


Apply Today

If you believe your experience aligns with the role, even if you do not meet every requirement, you are encouraged to apply. ICON values diverse talent and potential across all career levels.