Parexel hiring Clinical Research Associate I
- Company Overview
- Job Role & Responsibilities
- Key Monitoring Responsibilities
- Site Management & Compliance
- Documentation & Systems Oversight
- Cross-Functional Collaboration
- Eligibility / Qualifications
- Educational Background
- Experience Requirements
- Core Skills
- Location & Salary
- Job Location
- Salary Information
- Application Process
- Apply Here
- Selection Process
- FAQs
- Summary Table
Parexel hiring Clinical Research Associate I in Bengaluru for life science & pharmacy graduates. Apply now for CRA role in India.
Parexel is hiring a Clinical Research Associate I (CRA I) in Bengaluru for professionals who want to build a long-term career in global clinical research. This role is ideal for candidates with a life sciences, pharmacy, nursing, or healthcare background who are passionate about patient safety, regulatory compliance, and high-quality clinical trial execution. As one of the world’s leading Contract Research Organizations (CROs), Parexel offers structured career growth, exposure to international clinical trials, and hands-on responsibility across the full clinical trial lifecycle. This opportunity is especially valuable for candidates seeking stability, global exposure, and advancement in the pharmaceutical and clinical research industry.
Company Overview
Parexel is a globally recognized Contract Research Organization (CRO) providing end-to-end clinical research, regulatory consulting, and market access services to pharmaceutical, biotechnology, and medical device companies. With decades of experience and a presence across multiple continents, Parexel plays a critical role in accelerating drug development while maintaining the highest standards of patient safety, data integrity, and regulatory compliance.
Job Role & Responsibilities
The Clinical Research Associate I acts as the primary point of contact between Parexel and assigned investigator sites. This role carries full responsibility for site quality, compliance, and study delivery from site identification through study close-out.
Key Monitoring Responsibilities
- Serve as Parexel’s direct representative at assigned clinical trial sites.
- Ensure protocol adherence, data integrity, and patient safety throughout the study lifecycle.
- Perform qualification, initiation, monitoring, and close-out visits.
- Conduct remote monitoring visits and site contacts when required.
- Build strong working relationships with investigators and site staff.
Site Management & Compliance
- Evaluate site feasibility, staffing adequacy, and infrastructure readiness.
- Support sites with study systems access and project-specific training requirements.
- Identify, address, and resolve site-level issues including documentation gaps and compliance risks.
- Ensure accurate and timely completion of CRF data, query resolution, and SAE reporting.
- Assess site recruitment strategies and provide actionable recommendations to improve enrollment.
Documentation & Systems Oversight
- Maintain high-quality documentation in CTMS, EDC, IVRS, and other clinical systems.
- Review and manage regulatory documents and Trial Master File (TMF) submissions.
- Ensure sites remain inspection- and audit-ready at all times.
- Track investigational product accountability, storage, and return or destruction.
Cross-Functional Collaboration
- Participate in investigator meetings, audits, and regulatory inspections.
- Communicate study risks, delays, or compliance concerns with proposed mitigation strategies.
- Collaborate with study teams to meet milestones, budgets, and timelines.
- Delegate and oversee administrative tasks through support teams when applicable.
This role requires independence, sound judgment, strong communication skills, and the ability to manage multiple priorities while maintaining compliance with international clinical research standards.
Eligibility / Qualifications
Educational Background
Candidates must hold a degree in one of the following disciplines:
- Life Sciences
- Pharmacy (B.Pharm, M.Pharm, Pharm.D)
- Biological Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Nursing or equivalent healthcare qualification
Experience Requirements
- Site management or equivalent experience in clinical research preferred.
- Strong understanding of clinical trial methodology, monitoring processes, and regulatory requirements.
- Familiarity with ICH-GCP guidelines and global clinical trial regulations.
Core Skills
- Clinical trial monitoring and site management
- Risk-based monitoring principles
- Clinical documentation and TMF management
- CTMS, EDC, IVRS, and EDMS systems
- Strong analytical and problem-solving skills
- Excellent interpersonal, verbal, and written communication
- Ability to work independently in a matrix and virtual team environment
- Willingness to travel extensively as per study requirements
Location & Salary
Job Location
- Bengaluru, India
Salary Information
- Compensation is competitive and aligned with industry standards.
- Salary depends on prior clinical research experience, skill level, and role expectations.
- Additional benefits include performance-based growth, structured learning programs, and global project exposure.
Application Process
Interested candidates should apply online through the official Parexel careers portal.
Apply Here
https://jobs.parexel.com/en/job/-/-/877/89428918944
Selection Process
- Resume screening
- Interview rounds (technical and competency-based)
- Final selection based on experience, skill alignment, and project requirements
Applicants are advised to keep updated documentation related to clinical research experience, certifications, and education.
FAQs
1. Is this role suitable for entry-level candidates?
Yes, CRA I is suitable for candidates with foundational clinical research or site management experience.
2. Is travel required for this role?
Yes, extensive travel to investigator sites is required.
3. Does Parexel provide training for CRAs?
Yes, Parexel offers comprehensive onboarding and continuous learning programs.
4. Is ICH-GCP knowledge mandatory?
Yes, a strong understanding of ICH-GCP and regulatory compliance is essential.
5. What systems should a CRA be familiar with?
CTMS, EDC, IVRS, EDMS, and MS Office tools.
Summary Table
| Category | Details |
|---|---|
| Company | Parexel |
| Vacancies | Clinical Research Associate I |
| Required Education | Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Nursing |
| Experience | Clinical research or site management experience |
To apply for this job please visit jobs.parexel.com.
