Parexel Hiring Initiation Clinical Research Associate (iCRA)
- Parexel Hiring Initiation Clinical Research Associate (iCRA) – Clinical Trial Start-Up Roles in Bengaluru & Mumbai
- Company Overview
- Job Role & Responsibilities
- Initiation Clinical Research Associate (iCRA)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why This Role Matters in Pharma & Healthcare
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What does an iCRA do?
- What career growth can I expect?
- Is this a high-paying clinical research job?
- Summary
Parexel Hiring Initiation Clinical Research Associate (iCRA) – Clinical Trial Start-Up Roles in Bengaluru & Mumbai
Parexel is hiring Initiation Clinical Research Associate I (iCRA) professionals for its clinical research operations in Bengaluru and Mumbai. This is a full-time opportunity in clinical trial start-up and site activation for candidates with strong experience in regulatory submissions, site initiation processes, and clinical operations.
Multiple openings are expected for this role, targeting professionals with experience in clinical research, site activation, and regulatory documentation. This is a high-growth opportunity for candidates aiming to build a long-term career in clinical trials, CRO operations, and global drug development.
Company Overview
Parexel is a leading global clinical research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in bringing new therapies to market. The company is known for its expertise in clinical development, regulatory consulting, and patient-focused research.
With a strong global presence and decades of experience, Parexel plays a key role in accelerating drug approvals and ensuring compliance with international regulatory standards.
Job Role & Responsibilities
Initiation Clinical Research Associate (iCRA)
- Manage site start-up activities from site identification to activation
- Act as primary point of contact for investigator sites during start-up phase
- Prepare and submit regulatory documents (IRB/IEC, MoH submissions)
- Coordinate feasibility assessments, site qualification, and activation processes
- Review and approve essential documents including ICF and site readiness documents
- Maintain Trial Master File (TMF) and ensure first-time quality documentation
- Update Clinical Trial Management Systems (CTMS) and track timelines
- Identify risks in study start-up and proactively resolve issues
- Collaborate with cross-functional teams, sponsors, and stakeholders
- Ensure compliance with ICH-GCP guidelines and regulatory requirements
Eligibility / Qualifications
- Educational Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing or related health sciences
- Experience: Prior experience in clinical research, site start-up, or regulatory roles preferred
- Strong understanding of clinical trial processes, ICH-GCP, and regulatory submissions
- Experience with CTMS, eTMF, and clinical documentation systems
- Excellent communication, organizational, and problem-solving skills
Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, Nursing
Location & Salary
- Job Location: Bengaluru, Karnataka & Mumbai, Maharashtra, India
- Work Mode: Hybrid / On-site
- Salary Range: ₹6 LPA – ₹14 LPA (approximate based on CRA and start-up roles in CRO industry)
This range reflects the demand for clinical research associates involved in site activation and regulatory processes.
Application Process
Apply directly through the official Parexel careers portal:
Apply Here: https://jobs.parexel.com/en/job/-/-/877/94688060288
Early application is recommended due to high competition for CRA and clinical research roles.
Why This Role Matters in Pharma & Healthcare
Clinical Research Associates play a vital role in ensuring that clinical trials are conducted ethically, safely, and in compliance with regulatory standards. The start-up phase is critical in ensuring studies begin efficiently and meet global regulatory expectations.
This role provides exposure to global clinical trials, regulatory frameworks, and cross-functional collaboration, making it one of the most valuable career paths in clinical research.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, prior clinical research or start-up experience is preferred.
What does an iCRA do?
An iCRA manages site activation, regulatory submissions, and start-up processes for clinical trials.
What career growth can I expect?
You can grow into CRA II, Senior CRA, Clinical Project Manager, or Regulatory Lead roles.
Is this a high-paying clinical research job?
Yes, CRA roles offer strong salary growth and global career opportunities.
Summary
| Category | Details |
|---|---|
| Company | Parexel |
| Vacancies | Initiation Clinical Research Associate (iCRA) |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing |
| Experience | Clinical research / site start-up experience preferred |
To apply for this job please visit jobs.parexel.com.
