Parexel is hiring for Initiation Clinical Research Associate I (iCRA) in Bengaluru. This is a valuable pharma job opportunity in clinical research and study startup. Ideal for professionals seeking strong pharmaceutical careers in India with a global Clinical Research Organization.
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About the Company
Parexel is one of the world’s leading Contract Research Organizations (CROs), providing end-to-end clinical development solutions to biopharmaceutical and medical device companies.
With deep expertise across clinical trials, regulatory affairs, consulting, and market access, Parexel is known for its commitment to quality, innovation, and regulatory compliance. The company operates globally and helps bring life-changing therapies to patients faster while maintaining the highest ethical and scientific standards.
Job Details
- Company Name: Parexel
- Experience: Not specified (varies by role)
- Qualification: Not specified
- Location: Bengaluru, India
- Work Type: Full time (On-site)
Job Description
Parexel is seeking a motivated Initiation Clinical Research Associate I (iCRA) to support critical study startup activities. The role focuses on Pre-SIV (Site Initiation Visit) and activation tasks to ensure smooth and compliant initiation of clinical trials in India.
Initiation Clinical Research Associate I (iCRA)
- Department: Clinical Operations / Clinical Development
- Role: Initiation Clinical Research Associate I
- Experience: Not specified
- Education/Qualification: Not specified
Skills/Qualifications
- Strong understanding of clinical trial startup processes
- Knowledge of IRB/IEC submission and approval procedures
- Excellent documentation and review skills
- Understanding of essential documents (ICF, SRP, Site Greenlight, etc.)
- Ability to manage protocol amendments
- Good communication and coordination skills
- Familiarity with GCP and regulatory requirements
Key Responsibilities
- Manage Pre-SIV and site activation tasks
- Drive study startup strategy and execution
- Prepare initial site-related IRB applications
- Review and approve essential documents
- Support protocol amendment submissions
- Ensure timely site activation
- Coordinate with cross-functional teams
Benefits/Perks
- Career growth in global clinical research
- Learning opportunities in clinical trial management
- Collaborative and supportive work culture
- Global exposure to diverse therapeutic areas
- Competitive compensation and benefits
- Long-term professional development
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Parexel career page.
🔗 Click below to apply directly for this job
Interested candidates can apply directly through the official Parexel Careers portal using Job Requisition ID R0000041327. For more pharma jobs and clinical research opportunities across India, visit Pharma Recruiter.
Apply before the deadline and take your clinical research career to the next level!
Walk-in Interview Details
Not applicable (Online Application)
Why You Should Join
Parexel offers a purpose-driven culture where every employee contributes to improving global health. Joining as an iCRA gives you meaningful work, long-term career stability, continuous learning in clinical operations, and recognition for your contributions.
Work in a highly compliant, innovative environment alongside industry experts while gaining valuable international exposure in clinical trial delivery.
FAQs
Q1: What is the main focus of the iCRA role at Parexel?
A: The role primarily handles Pre-SIV, site activation, and startup activities for clinical trials.
Q2: Where is this Parexel job located?
A: Bengaluru, Karnataka (India).
Q3: What is the last date to apply?
A: May 8, 2026.
Q4: What are the growth opportunities at Parexel?
A: Excellent scope for advancement in Clinical Operations, exposure to global studies, and development into senior CRA roles.
