Parexel Hiring iCRA II | Clinical Research Jobs in Bengaluru
If you’re aiming to build a strong, future-proof career in clinical research jobs, here’s an exceptional opportunity at Parexel. The organization is hiring an iCRA II—a role that directly accelerates clinical trials, strengthens site operations, and contributes to bringing life-changing therapies to patients sooner. If you want to join a globally trusted CRO known for innovation, growth, and excellence, this opening in Bengaluru places you at the center of impactful work.
ABOUT THE COMPANY:
Parexel is one of the world’s leading Contract Research Organizations (CROs), supporting global biopharma clients in developing breakthrough treatments. With a commitment to quality, patient safety, scientific excellence, and regulatory integrity, Parexel offers unmatched opportunities for professionals seeking to grow in clinical research jobs, parexel jobs, and clinical data management jobs. Their diverse therapeutic exposure, collaborative culture, and global reach make Parexel a preferred employer for CRAs worldwide.
JOB DETAILS:
As an iCRA II, you serve as Parexel’s primary site-facing professional. This role is crucial in ensuring site quality, regulatory compliance, start-up efficiency, and patient safety throughout clinical trials. The position offers opportunities to work globally, handle complex study requirements, and grow professionally within broad therapeutic
areas.- Role: iCRA II (Intermediate Clinical Research Associate)
- Location: Bengaluru, India
- Industry: Global Clinical Trials & CRO Services
- Employer: Parexel
EDUCATIONAL REQUIREMENTS:
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Bachelor’s degree in Biological Sciences, Pharmacy, Nursing, or Health-related disciplines
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Equivalent clinical research experience may also be considered
KEY RESPONSIBILITIES:
Start-Up (Site Identification → Activation)
- Act as the direct Parexel point of contact for assigned investigator sites
- Support feasibility, pre-qualification, and qualification activities
- Manage Confidentiality Agreements, site contracts, and related documentation
- Prepare and submit IRB/IEC/MoH submissions
- Review & negotiate site-specific ICFs and amendments
- Ensure First Time Quality (FTQ) of all TMF documents
- Update CTMS and project systems in real time
- Resolve site start-up challenges and escalate risks proactively
Maintenance & Ongoing Monitoring
- Maintain regulatory communication and IRB/IEC submissions
- Manage site-level documentation updates and TMF completeness
- Support ongoing ICF updates, approvals, and regulatory amendments
- Ensure compliance with ICH-GCP, local laws, and Parexel SOPs
Overall CRA Responsibilities
- Conduct monitoring activities ensuring patient safety and data integrity
- Ensure sites are “audit-ready” at all times
- Maintain consistent, high-quality documentation
- Build strong relationships with investigators and site staff
- Communicate risks, milestones, and timelines to internal teams
- Mentor junior team members when needed
- Work cross-functionally across global study teams
- Complete administrative tasks such as timesheets, expenses, and metrics
SKILLS REQUIRED:
- Strong understanding of clinical trials terminology
- Excellent communication, presentation & interpersonal skills
- Ability to work independently with minimal supervision
- High attention to detail & strong analytical skills
- Problem-solving and critical decision-making abilities
- Ability to operate in a matrix team structure
- Proficiency in CTMS, eTMF, and MS Office
- Ability to multitask and manage shifting priorities
- Strong cultural adaptability; experience in virtual teamwork
- Client-focused, professional attitude
Stepping into the iCRA II role at Parexel is a powerful career move for anyone aiming to excel in clinical research jobs. With access to global studies, cross-functional collaboration, and continuous growth opportunities, Parexel empowers you to make a real difference in patient outcomes. If you’re ready to take the next step in your CRA journey, this is your moment.
