Clinical Research Associate (CRA) Job at Parexel – Apply Now
Parexel is hiring Clinical Research Associates (CRA) in Bengaluru, India, to play a crucial role in clinical trials and patient safety. As a CRA, you will monitor investigator sites, ensure regulatory compliance, and oversee clinical trial data integrity.
This position offers an exciting opportunity to work on global projects across therapeutic areas while developing your career in clinical research. If you have experience in site management, clinical trial methodology, and GCP compliance, apply today!
Clinical Research Associate (CRA) Job at Parexel – Apply Now!
Location: Bengaluru, India
About the Role
As a Clinical Research Associate (CRA) at Parexel, you will be responsible for monitoring clinical trial sites, ensuring compliance with study protocols, and maintaining data integrity. Your role will involve direct collaboration with investigators, site staff, and clinical research teams to ensure treatments reach patients faster while upholding the highest clinical and ethical standards.
Key Responsibilities
Clinical Trial Site Management (Initiation to Close-Out)
- Serve as Parexel’s primary contact with assigned clinical trial sites.
- Ensure study implementation aligns with protocols and regulatory requirements.
- Resolve site-related issues and provide compliance training.
- Evaluate on-site staff assignments and suggest corrective actions when necessary.
- Address and resolve data integrity and documentation issues.
- Monitor and manage clinical trial supply and compliance.
- Review and approve regulatory documents and site documentation.
Regulatory Compliance & Data Integrity
- Ensure compliance with ICH-GCP, local regulations, and Parexel SOPs.
- Conduct on-site visits and remote monitoring to ensure study accuracy.
- Oversee clinical trial management system (CTMS) updates.
- Maintain audit and inspection readiness of assigned sites.
- Track investigator payments and CRF data entry.
Team Collaboration & Reporting
- Collaborate with cross-functional teams to meet project goals.
- Provide strategies for project planning and site recruitment.
- Attend and contribute to investigator meetings, audits, and inspections.
- Ensure timely documentation and reporting of clinical trial data.
- Develop expertise to become a subject matter expert in clinical research.
Required Qualifications & Skills
Education: Degree in Biological Science, Pharmacy, Nursing, or related health discipline.
Experience & Knowledge:
- Prior site management or clinical research experience.
- Understanding of clinical trial methodology, ICH-GCP, and regulatory compliance.
- Experience with clinical trial management systems (CTMS) and electronic document management systems (EDMS).
Key Skills:
- Strong problem-solving and analytical skills.
- Excellent communication & interpersonal skills.
- Detail-oriented, organized, and proactive approach to work.
- Ability to work independently and in a global team environment.
- Advanced presentation skills and consulting abilities.
- Flexibility to travel extensively as required.
Why Join Parexel?
- Work on global clinical research projects in diverse therapeutic areas.
- Career growth opportunities in clinical research and drug development.
- Collaborate with experts in a supportive, innovation-driven environment.
- Play a crucial role in patient safety and treatment advancements.
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