Parexel is hiring an Initiation Clinical Research Associate I (iCRA) for its Bengaluru office. This role focuses on clinical trial startup, site activation, and regulatory submissions — a great opportunity for professionals seeking pharma jobs and pharmaceutical careers in India.
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About the Company
Parexel is a leading global Clinical Research Organization (CRO) with over 40 years of experience delivering clinical and consulting solutions to the life sciences industry. Renowned for its regulatory expertise, innovation, and patient-centric approach, Parexel partners with biopharmaceutical companies to accelerate clinical development.
The company maintains strong emphasis on quality, compliance, and operational excellence across global markets, offering outstanding career opportunities in clinical research.
Job Details
- Company Name: Parexel
- Position: Initiation Clinical Research Associate I (iCRA)
- Experience: Substantial start-up experience or equivalent in clinical research
- Qualification: Degree in biological science, pharmacy, or other health-related discipline
- Location: Bengaluru, India
- Work Type: Full time (On-site)
Job Description
Parexel is seeking a motivated Initiation Clinical Research Associate I to drive clinical trial startup and site activation activities in Bengaluru. The role is critical for ensuring timely, high-quality site initiation, regulatory submissions, and document management in compliance with ICH-GCP and sponsor requirements.
- Initiation Clinical Research Associate I Department: Clinical Operations / Site Startup
- Location: Bengaluru, India
- Role: Initiation Clinical Research Associate I (iCRA)
- Experience: Substantial clinical research startup experience
- Education/Qualification: Degree in biological science, pharmacy, or health-related field
Skills/Qualifications
- Degree in biological science, pharmacy, or health-related discipline
- Strong experience in clinical trial startup and site activation
- Excellent knowledge of ICH-GCP and regulatory requirements
- Proficiency in CTMS, eTMF, and MS Office tools
- Strong problem-solving, communication, and presentation skills
- Ability to work independently with minimal supervision
- Experience working in a matrix and multicultural environment
- Attention to detail and strong organizational skills
Key Responsibilities
- Manage site startup and activation activities end-to-end
- Build relationships with investigators and site staff
- Prepare and submit IRB/IEC and regulatory applications
- Customize and negotiate Informed Consent Forms (ICF)
- Ensure First Time Quality of essential documents
- Update CTMS and maintain Trial Master File (TMF)
- Support feasibility and site qualification activities
- Resolve site issues and escalate risks promptly
- Prepare sites for audits and inspections
- Facilitate training and system access for sites
Benefits/Perks
- Career growth in a global Clinical Research Organization
- Exposure to diverse clinical trial projects
- Learning opportunities in regulatory and startup processes
- Collaborative and supportive work culture
- Global project exposure and mentorship
- Professional development in clinical operations
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.
Apply here: Parexel Careers
For more pharma jobs, clinical research openings, and pharmaceutical careers in India, visit Pharma Recruiter. Apply promptly to secure your opportunity.
Why You Should Join
Parexel fosters a high-performance culture with strong values of empathy, integrity, and innovation. As an iCRA, you will play a meaningful role in bringing new therapies to patients while gaining valuable experience in clinical trial startup. The company offers long-term career stability, continuous learning, and a supportive environment committed to regulatory excellence and operational quality.
FAQs
Q1: What qualifications are required for the Initiation Clinical Research Associate I role?
A: A degree in biological science, pharmacy, or health-related discipline with substantial clinical trial startup experience.
Q2: Where is the job located?
A: The position is based in Bengaluru (Bangalore), India.
Q3: What does the iCRA role mainly focus on?
A: It focuses on clinical trial startup, site activation, IRB submissions, and essential document management.
Q4: Is this a good opportunity for pharmaceutical careers in India?
A: Yes. It provides strong exposure in clinical operations within a reputed global CRO, enhancing long-term career prospects.
