Hybrid Clinical Research Associate Job at ICON plc
Looking for a promising career in clinical research? Here is an exciting opportunity for experienced professionals to join ICON plc as a CRA I / II in Mumbai. This hybrid Clinical Research Associate Job offers exposure to global clinical trials, oncology and immunology therapeutic areas, and advanced clinical monitoring activities. Candidates with strong on-site monitoring experience and knowledge of ICH-GCP guidelines can explore this opportunity to grow in the clinical development industry.
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovation, excellence, and advancing clinical development. The company works with global healthcare partners to support clinical trials and innovative therapies across multiple therapeutic areas. ICON plc promotes an inclusive work culture and provides employees with opportunities to contribute to impactful clinical research programs worldwide.
Job Details:
- Job Role: CRA I / II
- Location: Mumbai
- Job Reference Number: JR135624
- Work Mode: Hybrid
- Department: Clinical Monitoring – ICON Strategic Solutions (FSP)
Clinical Monitoring Job Responsibilities
Candidates selected for this Clinical Research Associate Job will be responsible for various site monitoring and trial management activities.
Key Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, patient safety, and data integrity
- Collaborate with investigators and site staff for smooth trial conduct
- Perform data review and query resolution activities
- Contribute to preparation and review of study documentation
- Support clinical study reports and protocol-related documentation
This Clinical Research Associate Job requires strong attention to detail and the ability to manage clinical trial activities efficiently.
Eligibility Criteria for Clinical Research Associate Job
Educational Qualification
- Bachelor’s degree in a scientific or healthcare-related field
Experience Required
- Minimum 3 years of experience as a Clinical Research Associate
- Experience in On-Site Monitoring is mandatory
Mandatory Skills
- In-depth knowledge of clinical trial processes and ICH-GCP guidelines
- Oncology/Immunology therapeutic area experience is mandatory
- Strong communication and organizational skills
- Ability to work independently and in collaborative environments
- Ability to travel at least 60% of the time
- Valid driver’s license required
Employee Benefits at ICON plc
ICON plc offers multiple employee-focused benefits for work-life balance and professional well-being.
Benefits Include
- Competitive salary
- Annual leave entitlements
- Health insurance offerings
- Retirement planning benefits
- Employee Assistance Programme (LifeWorks)
- Life assurance
- Flexible country-specific benefits
- Childcare vouchers and travel pass support
- Discounted gym memberships and health assessments
