Parexel Hiring Initiation Clinical Research Associate I in Bengaluru | Clinical Research Jobs 2026
Parexel Hiring Initiation Clinical Research Associate I in Bengaluru | Clinical Research Jobs 2026
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(Parexel Hiring Initiation Clinical Research Associate I) |
Introduction
The clinical research industry in India is expanding rapidly, creating excellent opportunities for professionals interested in clinical operations, regulatory submissions, and site start-up activities. Parexel, one of the world’s leading Clinical Research Organizations (CROs), has announced a new opening for the position of Initiation Clinical Research Associate I (iCRA) in Bengaluru, India.
This role is ideal for candidates who want to build long-term careers in:
- Clinical trial start-up
- Clinical operations
- Regulatory affairs
- Site activation
- TMF management
- Global clinical research
Candidates with experience in:
- IRB/IEC submissions
- CTMS systems
- eTMF documentation
- Clinical trial compliance
- Site management
can explore this exciting opportunity with Parexel.
The position offers strong career growth, global clinical trial exposure, and the opportunity to work with one of the most respected organizations in the pharmaceutical and healthcare research industry.
About Parexel
Parexel is a globally recognized Clinical Research Organization (CRO) specializing in clinical development, regulatory consulting, and market access services for pharmaceutical, biotechnology, and medical device companies.
The company supports drug development programs across multiple therapeutic areas and helps sponsors accelerate clinical research through advanced operational and regulatory solutions.
Company Overview
Company Name: Parexel
Industry: Clinical Research / CRO / Drug Development
Headquarters: Durham, North Carolina, United States
Founded: 1982
Global Presence: 100+ Countries
Employees: 20,000+ Worldwide
Parexel is known for:
- Global clinical trial management
- Regulatory consulting services
- Clinical operations excellence
- Patient-focused drug development
- Advanced healthcare innovation
The company works with many leading pharmaceutical and biotechnology companies globally.
Job Overview Summary
Parexel is hiring an Initiation Clinical Research Associate I (iCRA) for its Bengaluru operations. The selected candidate will support clinical trial start-up activities, regulatory submissions, site activation processes, TMF documentation, and CTMS updates for global clinical studies.
This role provides excellent exposure to:
- International clinical trials
- Regulatory compliance systems
- Clinical site management
- Start-up operations
- Clinical trial documentation
Professionals interested in clinical operations and site activation careers can significantly grow their expertise through this opportunity.
Vacancy Details
Job Information
Position: Initiation Clinical Research Associate I (iCRA)
Company: Parexel
Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Industry: Clinical Research / CRO
Application Deadline: May 15, 2026
Estimated Salary: ₹6.5 LPA – ₹10 LPA
Experience Required: Clinical research or start-up experience preferred
Job Role Explanation
The Initiation Clinical Research Associate I will support the initiation and activation of clinical trial sites before patient enrollment.
The role mainly focuses on:
- Site activation
- Regulatory submissions
- Trial documentation management
- Clinical site communication
- CTMS and eTMF maintenance
The selected candidate will coordinate with:
- Investigators
- Site staff
- Regulatory teams
- Clinical operations teams
- Sponsors and stakeholders
to ensure the smooth start-up of global clinical trials.
Key Responsibilities Explained
Clinical Trial Start-Up Activities
The candidate will manage:
- Site activation tasks
- Pre-SIV activities
- Regulatory approvals
- Site readiness activities
This ensures clinical sites are fully prepared before study initiation.
IRB/IEC Submissions
The role involves preparing and managing:
- IRB submissions
- IEC approvals
- Ethics committee documentation
- Regulatory communication
Proper submission handling is critical for regulatory compliance.
TMF & CTMS Management
The selected professional will maintain:
- Trial Master File (TMF)
- eTMF systems
- Clinical Trial Management Systems (CTMS)
Accurate documentation management helps maintain audit readiness and study quality.
Site Communication & Coordination
The iCRA will act as the primary contact for clinical sites and investigators.
Responsibilities include:
- Resolving site queries
- Managing communication timelines
- Supporting investigator relationships
- Coordinating compliance activities
Strong stakeholder management skills are important for this role.
Compliance & Quality Management
The role requires maintaining compliance with:
- ICH-GCP guidelines
- Regulatory standards
- Sponsor requirements
- Clinical trial SOPs
The candidate will also support audit and inspection readiness activities.
Eligibility Criteria
Candidates applying for this Parexel Clinical Research job should meet the following qualifications:
Educational Qualification
Bachelor’s Degree in:
- Life Sciences
- Pharmacy
- Nursing
- Biotechnology
- Healthcare-related fields
Experience Required
Candidates with:
- Clinical research experience
- Site start-up experience
- Regulatory documentation experience
will be preferred.
Knowledge of:
- IRB/IEC processes
- Clinical trial regulations
- CTMS systems
- eTMF workflows
is beneficial.
Skills Required
Technical Skills
- Clinical trial start-up knowledge
- CTMS expertise
- eTMF management
- Regulatory submissions
- Site activation activities
- TMF maintenance
- Clinical operations workflows
Soft Skills
- Communication skills
- Time management
- Problem-solving abilities
- Analytical thinking
- Stakeholder management
- Attention to detail
Candidates who can work effectively in matrix and global teams will have an advantage.
Salary Estimate
Based on current CRO industry trends in India, the estimated salary for this role may range between:
₹6,50,000 – ₹10,00,000 per annum
Salary may vary depending on:
- Experience level
- Clinical research expertise
- Start-up operations knowledge
- CTMS and TMF skills
- Communication abilities
Why Join Parexel?
Working at Parexel offers strong career opportunities in global clinical research operations.
Employee Benefits
- Exposure to international clinical trials
- Opportunity to work with global sponsors
- Advanced CRO environment
- Professional learning and development
- Career growth in clinical operations
- Collaborative work culture
- Experience in global regulatory processes
This role can significantly help professionals build expertise in:
- Clinical trial start-up
- Site activation
- Regulatory affairs
- Clinical operations management
Interview Details
Currently, Parexel has not officially announced walk-in interview details for this role.
Candidates should:
- Apply online through the official application portal
- Keep updated resumes ready
- Monitor email communication regularly
The recruitment process may include:
- HR screening
- Technical interview
- Clinical operations discussion
- Final managerial round
Required Documents
Candidates should keep the following documents ready during the application process:
- Updated Resume/CV
- Educational Certificates
- Government ID Proof
- Experience Certificates
- Current Salary Details
- Last Salary Slips
- Clinical project experience details
- CTMS/eTMF knowledge information
Proper documentation may improve the interview and shortlisting process.
Job Location
Location: Bengaluru, Karnataka, India
Work Mode: Full-Time
Industry: Clinical Research / CRO / Clinical Operations
Bengaluru is one of India’s leading healthcare and clinical research hubs, offering strong career opportunities in the pharmaceutical and CRO industries.
How to Apply
Application Link:
Candidates are advised to apply through the official Parexel career portal before the application deadline.
Frequently Asked Questions (FAQs)
Q1. What is the job location for the Parexel iCRA role?
The job location is Bengaluru, Karnataka, India.
Q2. What is the role offered by Parexel?
Parexel is hiring for the Initiation Clinical Research Associate I (iCRA) position.
Q3. What qualifications are required for this role?
Candidates with degrees in Life Sciences, Pharmacy, Nursing, or related healthcare fields can apply.
Q4. What skills are important for this role?
Important skills include:
- CTMS knowledge
- TMF management
- Regulatory submissions
- Clinical trial start-up operations
- Site activation experience
Q5. What is the estimated salary for this role?
The estimated salary range is ₹6.5 LPA – ₹10 LPA.
Q6. Is prior clinical research experience required?
Yes, candidates with clinical research or site start-up experience are preferred.
Final Conclusion
Parexel’s latest hiring for the Initiation Clinical Research Associate I role in Bengaluru is an excellent opportunity for candidates looking to build strong careers in clinical trial start-up operations and global clinical research.
With increasing global demand for:
- Clinical operations professionals
- Regulatory specialists
- Site activation experts
- CTMS and TMF professionals
Clinical research careers continue to offer excellent long-term growth opportunities in India.
Candidates with strong knowledge of:
- Clinical trial documentation
- Site activation workflows
- IRB/IEC processes
- Regulatory compliance
- Clinical operations systems
can build rewarding careers with global CRO leaders like Parexel.
This opportunity is especially valuable for professionals who want exposure to:
- International clinical trials
- Global healthcare regulations
- Advanced CRO systems
- High-quality clinical operations environments
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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