Are you looking for an exciting career as a Clinical Research Associate (CRA) in India? Parexel, a leading global clinical research organization (CRO), is hiring a CRA in Bengaluru to contribute to groundbreaking clinical trials and help bring life-saving treatments to patients faster.
If you have a background in clinical research, life sciences, or pharmacy, this could be the perfect opportunity for you. Read on to learn more about the CRA job role, responsibilities, qualifications, and how to apply.
Job Overview – Clinical Research Associate (CRA) at Parexel
As a Clinical Research Associate (CRA) at Parexel, you will play a crucial role in monitoring clinical trial sites, ensuring compliance with protocols, and safeguarding patient safety. You will work closely with investigators, site staff, and cross-functional teams to ensure smooth trial execution.
Key Responsibilities:
- Conduct site qualification, initiation, monitoring, and close-out visits (on-site & remote).
- Ensure regulatory compliance with ICH-GCP, local regulations, and Parexel SOPs.
- Review and verify clinical trial data for accuracy and integrity.
- Build strong relationships with investigators and site staff to enhance trial efficiency.
- Identify and resolve site-related issues promptly to avoid delays.
- Maintain Trial Master Files (TMF) and ensure proper documentation.
- Participate in audits, inspections, and investigator meetings as required.
- Support patient recruitment strategies and site performance improvements.
Skills & Qualifications Required for CRA Role
Education & Experience:
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
- 1-3 years of experience as a CRA or in clinical research (site management, monitoring, or coordination).
- Strong knowledge of ICH-GCP guidelines, clinical trial protocols, and regulatory requirements.
Essential Skills:
- Excellent communication & interpersonal skills for effective site interactions.
- Strong problem-solving & analytical abilities to address trial challenges.
- Attention to detail for accurate data review and documentation.
- Proficiency in Clinical Trial Management Systems (CTMS), EDC, and MS Office.
- Ability to travel frequently to investigator sites as needed.
Why Join Parexel as a CRA?
Parexel is a top-rated CRO known for its employee-friendly culture, career growth opportunities, and impactful work in clinical research. Here’s why you should apply:
✅ Global Exposure: Work on international clinical trials across multiple therapeutic areas.
✅ Career Growth: Opportunities to upskill and advance in clinical research.
✅ Work-Life Balance: Flexible work policies and supportive team environment.
✅ Competitive Salary & Benefits: Attractive compensation package with health benefits.
How to Apply for the CRA Position at Parexel
If you meet the qualifications and are excited about this Clinical Research Associate job in Bengaluru, follow these steps:
- Click on the “Apply Now” button on the Parexel careers page.
- Submit your updated resume highlighting your clinical research experience.
- Prepare for interviews – Be ready to discuss your monitoring experience, GCP knowledge, and problem-solving skills.
📍 Location: Bengaluru, India
