Clinical Research Associate II at ICON plc India | Remote + Travel | 2+ Yrs
Clinical Research Associate II at ICON plc India | Remote + Travel | 2+ Yrs

Clinical Research Associate II Position at ICON plc India

A rare chance has emerged for experienced clinical research professionals as ICON plc is actively hiring for the position of Clinical Research Associate II (CRA II) in India. This role offers flexible remote working and travel opportunities, making it an appealing option for those with at least 2 years of CRA experience.

About ICON plc

ICON plc is a globally recognized clinical research organization (CRO) specializing in healthcare intelligence, clinical development, and data-driven solutions. With operations across multiple countries, ICON supports pharmaceutical, biotechnology, and medical device companies in bringing innovative therapies to market. The company is known for its strong focus on clinical trial excellence, regulatory compliance, and patient safety. ICON provides end-to-end clinical research services, making it a preferred employer for professionals in pharmacovigilance, clinical operations, and regulatory affairs.

Company: ICON plc

Job Title: Clinical Research Associate II

Job Location: Remote, with travel across India

Experience Required: Minimum 2 years as a Clinical Research Associate

Clinical Research Associate II Job Description

As a Clinical Research Associate II, the individual will be responsible for managing clinical trial sites and ensuring high-quality study execution. This role plays a critical part in ensuring that clinical trials meet global regulatory standards and deliver reliable results.

Key Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits
  • Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
  • Monitor patient safety and maintain data integrity throughout clinical trials
  • Review clinical data and resolve queries in collaboration with site teams
  • Coordinate with investigators, sponsors, and cross-functional teams
  • Support preparation and review of clinical trial documentation and reports
  • Maintain accurate trial records in systems such as CTMS and eTMF

Eligibility Criteria

  • Educational Qualification: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
  • Relevant Courses: B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Clinical Research, Biotechnology, Microbiology, Biochemistry, Nursing, Clinical Data Management
  • Experience: Minimum 2 years of experience as a Clinical Research Associate

Required Skills

  • Strong understanding of clinical trial processes and ICH-GCP guidelines
  • Excellent communication and stakeholder management skills
  • Ability to manage multiple sites and timelines effectively
  • Strong analytical and problem-solving capabilities
  • Willingness to travel up to 60%

Salary and Benefits

Salary: Competitive salary package with performance-based benefits

Benefits: Health insurance and wellness programs, retirement and financial planning support, paid leaves and work-life balance initiatives, employee assistance programs and global support services.

How to Apply

Candidates can apply directly through the official ICON careers page: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Conclusion

This opportunity at ICON plc for the Clinical Research Associate II role presents a significant career advancement for qualified candidates. Interested individuals are encouraged to apply before the deadline to seize this chance to contribute to impactful clinical research.

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