ICON Plc Hiring Clinical Research Associate
- ICON Hiring CRA I / CRA II – Oncology Clinical Monitoring | 3+ Years Experience | Mumbai | Hybrid
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Required Skills
- Location & Salary
- Benefits & Rewards
- Why This Role Is Critical in Clinical Development
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What experience is required for CRA I / II at ICON?
- 2. Is oncology experience mandatory?
- 3. Is this a remote position?
- 4. How much travel is involved?
- 5. What career growth opportunities are available?
- Recruitment Summary
ICON Hiring CRA I / CRA II – Oncology Clinical Monitoring | 3+ Years Experience | Mumbai | Hybrid
ICON Strategic Solutions is hiring for the position of Clinical Research Associate (CRA I / CRA II) under the Clinical Monitoring division in Mumbai. This is a hybrid opportunity for experienced professionals with a minimum of 3 years of on-site monitoring experience in clinical trials, particularly within Oncology or Immunology therapeutic areas.
If you are an experienced CRA looking to work with a global clinical research organization and contribute to complex, high-value clinical trials, this role offers strong exposure to international studies, regulatory compliance, and advanced clinical development programs.
Company Overview
ICON plc is a globally recognized healthcare intelligence and clinical research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in accelerating drug development. With a strong global footprint, ICON delivers clinical trial management, regulatory consulting, data management, and clinical monitoring services across multiple therapeutic areas.
The organization partners with leading sponsors to design, manage, and analyze Phase I–IV clinical trials. ICON’s expertise in oncology, immunology, rare diseases, and advanced therapeutics positions it as a trusted name in clinical research and healthcare innovation.
By combining scientific expertise with data-driven clinical operations, ICON contributes directly to bringing innovative therapies to patients worldwide.
Job Role & Responsibilities
As a CRA I / CRA II, you will play a central role in monitoring clinical trials, ensuring regulatory compliance, and maintaining high standards of patient safety and data integrity.
Key Responsibilities
- Conduct site qualification, initiation, routine monitoring, and close-out visits.
- Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
- Oversee patient safety, informed consent processes, and source data verification.
- Perform data review and resolve clinical data queries in collaboration with site staff.
- Maintain accurate documentation including monitoring reports and essential study files.
- Collaborate with investigators, study coordinators, and cross-functional teams.
- Contribute to protocol review and clinical study documentation.
This role requires strong site management skills, regulatory knowledge, and the ability to handle complex oncology or immunology studies with precision.
Eligibility / Qualifications
Educational Qualification
Bachelor’s degree in a scientific or healthcare-related field.
Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Nursing, MSc Nursing, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Medical Laboratory Technology, Biomedical Sciences.
Experience
- Minimum 3 years of experience as a Clinical Research Associate with on-site monitoring exposure.
- Mandatory experience in Oncology or Immunology therapeutic area.
- Strong understanding of clinical trial processes and regulatory frameworks.
Required Skills
- In-depth knowledge of ICH-GCP guidelines and global clinical regulations.
- Experience in site monitoring, source data verification, and regulatory documentation.
- Strong organizational and communication skills.
- Ability to work independently in a fast-paced clinical research environment.
- Willingness to travel up to 60% (domestic and international) with a valid driver’s license.
Professionals with exposure to global trials, sponsor interactions, and regulatory inspections will have an advantage.
Location & Salary
Location: Mumbai, India
Work Model: Hybrid
Department: Clinical Monitoring
Salary details are not publicly disclosed. ICON offers competitive compensation aligned with industry standards for experienced CRAs in oncology clinical research, along with comprehensive employee benefits.
Benefits & Rewards
ICON emphasizes performance-driven growth and employee well-being. Benefits may include:
- Competitive salary packages.
- Health insurance options for employees and families.
- Retirement planning programs.
- Annual leave entitlements.
- Global Employee Assistance Program.
- Flexible benefits based on country policies.
The organization promotes diversity, inclusion, and equal opportunity employment.
Why This Role Is Critical in Clinical Development
Clinical Research Associates are the backbone of clinical trial execution. They ensure protocol adherence, patient safety, regulatory compliance, and high-quality data collection. In oncology and immunology studies, where treatment protocols are complex and patient populations are sensitive, strong monitoring expertise directly impacts trial success and regulatory approval timelines.
This position allows experienced CRAs to work on advanced therapies and innovative treatment strategies that may shape the future of global healthcare.
Application Process
Interested candidates can apply directly through the official ICON careers portal using the link below:
Ensure your resume clearly highlights oncology/immunology monitoring experience, ICH-GCP knowledge, and site management expertise.
Frequently Asked Questions (FAQs)
1. What experience is required for CRA I / II at ICON?
A minimum of 3 years of on-site clinical monitoring experience is required.
2. Is oncology experience mandatory?
Yes. Experience in Oncology or Immunology therapeutic areas is mandatory.
3. Is this a remote position?
No. The role follows a hybrid model and requires significant travel.
4. How much travel is involved?
Up to 60% domestic and international travel is required.
5. What career growth opportunities are available?
This role can lead to Senior CRA, Lead CRA, Clinical Trial Manager, or Project Management positions within global clinical research organizations.
Recruitment Summary
| Company | ICON Strategic Solutions |
|---|---|
| Vacancies | CRA I / CRA II – Clinical Monitoring |
| Required Education | Bachelor’s in Scientific or Healthcare Field |
| Experience | Minimum 3 Years On-Site Monitoring (Oncology/Immunology Mandatory) |
To apply for this job please visit careers.iconplc.com.
