ICON Clinical Research Associate Jobs in Mumbai present an excellent opportunity for professionals interested in clinical research, clinical monitoring, and pharmaceutical trial management. ICON is hiring Clinical Research Associate I / II professionals who will play a key role in monitoring clinical trials, ensuring compliance with global regulations, and maintaining data integrity.
If you have experience in clinical trials, oncology studies, ICH-GCP guidelines, and clinical monitoring, this role offers the chance to work with a leading global clinical research organization while contributing to the development of innovative therapies and life-saving treatments.
About ICON plc
ICON plc is a globally recognized healthcare intelligence and clinical research organization that provides outsourced development services to pharmaceutical, biotechnology, and medical device companies. The organization focuses on accelerating clinical development and improving healthcare outcomes worldwide.
With operations across multiple countries, ICON works closely with sponsors, investigators, and healthcare professionals to conduct clinical trials that meet global regulatory standards. The company promotes innovation, diversity, and collaboration while advancing medical science and patient care.
Icon CRA Job Details Overview
| Job Title | Clinical Research Associate I / II |
| Company Name | ICON plc |
| Location | Mumbai, India |
| Employment Type | Full Time |
| Application Deadline | Not Mentioned |
| Category | Latest Pharma Walk-in Interview |
CRA Job Responsibilities
- Conduct site qualification visits, initiation visits, monitoring visits, and close-out visits for clinical trials.
- Ensure that clinical studies are conducted in compliance with study protocols, regulatory requirements, and ICH-GCP guidelines.
- Maintain data integrity and ensure the safety and rights of patients participating in clinical trials.
- Collaborate with investigators and site staff to facilitate smooth clinical study execution.
- Review clinical data and resolve queries to ensure high-quality and accurate reporting.
- Prepare and review clinical documentation including protocols, monitoring reports, and study reports.
- Maintain regular communication with clinical trial teams and stakeholders.
- Ensure proper documentation and compliance throughout the clinical study lifecycle.
Required Qualifications & Skills For Clinical Research Associate
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 3 years of experience as a Clinical Research Associate with On-Site Monitoring experience.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Oncology/Immunology TA is mandatory.
- Strong organizational and communication skills with attention to detail.
- Ability to work independently as well as collaboratively in a dynamic environment.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.
Preferred / Bonus Skills
- Previous experience in global oncology clinical trials.
- Experience managing investigator sites and clinical monitoring activities.
- Strong problem-solving and analytical skills.
- Ability to manage multiple projects and deadlines simultaneously.
- Experience working in CRO or pharmaceutical clinical research environments.
Salary & Benefits
The salary for the Clinical Research Associate position is as per company norms. ICON also offers a competitive benefits package designed to support employee well-being and professional growth.
- Competitive salary structure
- Health insurance options
- Retirement planning benefits
- Global employee assistance program
- Annual leave and work-life balance initiatives
- Career development and training opportunities
ICON CRA I II Post Details
Post
Clinical Research Associate I / II
Department
Clinical Monitoring
Qualification & Experience
- Bachelor’s degree in a scientific or healthcare related field
- Minimum 3 years Clinical Research Associate experience
- Strong knowledge of ICH-GCP and clinical trial processes
Job Responsibility and Skill
- Clinical trial monitoring and site management
- Ensuring compliance with study protocols and regulatory guidelines
- Clinical data review and documentation management
- Coordination with investigators and study teams
How to Apply
Candidates interested in this clinical research opportunity can apply through the official application portal by following the steps below:
- Click the Apply Now button below.
- Open the job application page in a new tab.
- Review the job requirements and responsibilities.
- Submit your updated resume and relevant details.
- Complete the online application process.
Interview Tips for Clinical Research Associate Jobs
- Review clinical trial processes, ICH-GCP guidelines, and monitoring procedures before attending interviews.
- Prepare examples of previous clinical monitoring or trial management experience.
- Understand oncology clinical trials and regulatory compliance requirements.
- Demonstrate strong communication and organizational skills during the interview.
- Be ready to discuss your experience with site visits, data verification, and study documentation.
Career Growth & Related Opportunities
Clinical Research Associate roles provide excellent career progression within the clinical research industry. With experience and strong performance, professionals may advance to higher roles such as:
- Senior Clinical Research Associate
- Lead CRA
- Clinical Trial Manager
- Clinical Operations Manager
- Global Project Manager in Clinical Research
Working with global CRO organizations like ICON can also open doors to international clinical research projects and leadership opportunities.
ICON Clinical Research Associate Jobs Mumbai – FAQs
What qualification is required for ICON Clinical Research Associate jobs?
Candidates must have a bachelor's degree in a scientific or healthcare related field and experience in clinical research monitoring.
How much experience is required for CRA I / II roles?
The position requires a minimum of 3 years of experience as a Clinical Research Associate with on-site monitoring experience.
Is oncology experience required for this job?
Yes, Oncology or Immunology therapeutic area experience is mandatory for this role.
Is travel required for Clinical Research Associate roles?
Yes, candidates should be willing to travel approximately 60% of the time for clinical trial monitoring visits.
Where is the job location for this position?
The Clinical Research Associate role is based in Mumbai, India.
Conclusion
The ICON Clinical Research Associate I / II job in Mumbai is a promising opportunity for professionals in the clinical research and pharmaceutical industry. This role allows candidates to contribute to global clinical trials while developing expertise in monitoring, compliance, and clinical operations.
If you have experience in clinical trials and oncology studies, applying for this position can help you advance your career within a globally recognized CRO organization.
