Apply for ICON Hiring CRA II Jobs 2026 in India. Explore Clinical Research Jobs 2026 with strong growth opportunities today.
Introduction
ICON is currently hiring for the position of Clinical Research Associate II (CRA II) across Bengaluru, Chennai, and Trivandrum locations in India. This exciting opportunity is ideal for experienced clinical research professionals looking to advance their careers with a globally recognized clinical research organization. Candidates with experience in clinical trial monitoring, site management, regulatory compliance, and data integrity can apply for this role. If you are searching for Clinical Research Jobs, Pharma Jobs 2026, or Regulatory Affairs Jobs within a leading CRO, this vacancy offers excellent career growth, competitive benefits, and exposure to global clinical development programs.
About Company
ICON plc is a leading global healthcare intelligence and clinical research organization dedicated to accelerating the development of innovative medicines and therapies worldwide. The company partners with pharmaceutical, biotechnology, medical device, and government organizations to support clinical development from early-stage research through commercialization.
With operations spanning multiple countries, ICON provides a comprehensive range of services including clinical trial management, data management, biostatistics, regulatory consulting, pharmacovigilance, and healthcare intelligence solutions. The organization plays a critical role in helping sponsors bring life-saving treatments to patients faster while maintaining the highest standards of quality, ethics, and regulatory compliance.
Known for its scientific expertise and patient-focused approach, ICON continues to support groundbreaking research across therapeutic areas and remains one of the most respected names in the global clinical research industry.
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Job Details / Job Summary
| Particulars | Details |
|---|---|
| Company Name | ICON |
| Job Role | Clinical Research Associate II (CRA II) |
| Department | Clinical Research |
| Qualification Required | Bachelor’s Degree in Scientific or Healthcare-related Field |
| Experience Required | Minimum 2 Years |
| Salary Package | Competitive Salary with Performance Incentives |
| Job Location | Bengaluru, Chennai, Trivandrum |
| Employment Type | Full-Time |
| Industry Type | Clinical Research Organization (CRO) |
| Shift Timing | General Shift |
| Gender Eligibility | Male & Female |
| Application Mode | Online |
| Selection Process | Application Screening, Technical Interview, HR Interview |
| Skills Required | Clinical Monitoring, ICH-GCP, Site Management, Clinical Trial Operations |
| Official Notification Status | Active |
| Application Last Date | As Per Official Notification |
Eligibility Criteria
Candidates interested in this Clinical Research Jobs opportunity should meet the following requirements:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a healthcare-related discipline.
- Minimum 2 years of experience as a Clinical Research Associate.
- Strong knowledge of clinical trial operations and study management.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements.
- Experience conducting site monitoring visits and site management activities.
- Excellent communication and interpersonal skills.
- Ability to work independently and within cross-functional teams.
- Willingness to travel up to 60% for domestic and international assignments.
- Valid driving license preferred as per job requirements.
Required Skills
The ideal candidate should possess the following professional competencies:
- Clinical Trial Monitoring
- Site Qualification and Site Initiation Visits
- Site Close-Out Activities
- ICH-GCP Compliance
- Clinical Data Review
- Query Resolution Management
- Patient Safety Monitoring
- Regulatory Compliance
- Clinical Documentation Review
- Investigator and Site Relationship Management
- Risk-Based Monitoring
- Time Management and Organization Skills
- Clinical Research Operations
- Communication and Presentation Skills
- Problem-Solving and Analytical Thinking
These skills are highly relevant for Clinical Research Jobs, Pharmacovigilance Jobs, Regulatory Affairs Jobs, and other life sciences career opportunities.
Roles and Responsibilities
The selected Clinical Research Associate II will be responsible for:
- Conducting site qualification, initiation, routine monitoring, and close-out visits.
- Ensuring adherence to study protocols and applicable regulations.
- Monitoring patient safety and study conduct throughout clinical trials.
- Verifying source documentation and maintaining data quality standards.
- Collaborating with investigators, site coordinators, and research teams.
- Reviewing clinical data and resolving study-related queries.
- Ensuring timely reporting of study activities and site performance.
- Supporting protocol implementation and study startup activities.
- Maintaining accurate monitoring reports and trial documentation.
- Assisting in preparation and review of clinical study documents.
- Identifying compliance issues and recommending corrective actions.
- Contributing to successful execution of clinical development programs.
Salary Details
ICON offers an attractive compensation package based on industry standards and candidate experience.
Expected Benefits
- Competitive annual salary package
- Performance-based incentives
- Medical and health insurance benefits
- Retirement and pension plans
- Life insurance and disability coverage
- Employee wellness programs
- Learning and development opportunities
- Career progression and global exposure
- Structured training and professional development programs
Final compensation may vary depending on qualifications, experience, and business requirements.
Selection Process
The recruitment process generally involves the following stages:
Step 1: Online Application
Candidates must submit their applications through the official ICON careers portal.
Step 2: Resume Screening
Recruitment teams review applications based on qualifications and clinical research experience.
Step 3: Technical Assessment
Shortlisted candidates may undergo technical interviews focusing on clinical trial operations, monitoring experience, and GCP compliance.
Step 4: HR Interview
Selected candidates participate in an HR discussion covering compensation, availability, and organizational fit.
Step 5: Final Offer
Successful candidates receive an official employment offer after completion of all evaluation stages.
How to Apply
Interested candidates can apply online by following these steps:
- Visit the official ICON Careers website.
- Search for the CRA II job opening.
- Review eligibility criteria and job requirements carefully.
- Complete the online application form.
- Upload an updated resume and supporting documents.
- Submit the application before the position closes.
- Check your email regularly for recruitment updates.
Candidates seeking Latest Pharma Jobs, Clinical Research Jobs, B.Pharm Jobs, M.Pharm Jobs, and Pharma Company Hiring opportunities should apply as early as possible.
Frequently Asked Questions
1. What qualification is required for the CRA II position?
Candidates must hold a Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a healthcare-related field.
2. Can freshers apply for this role?
No. The position requires a minimum of 2 years of experience as a Clinical Research Associate.
3. What salary is offered for the CRA II role?
The company offers a competitive salary package along with performance incentives and employee benefits.
4. How can I apply for this Clinical Research job?
Candidates can apply through the official ICON careers portal by completing the online application process.