Are you a highly motivated and experienced Clinical Research Associate (CRA) looking for a new challenge? Do you have a strong understanding of GCP, ICH guidelines, and regulatory processes? If so, we have exciting news for you! CBCC Global Research, a leading player in the clinical research industry, is hiring experienced CRAs to join their team in Delhi, Bengaluru, Pune, and Kolkata.
About the Job
As a Clinical Research Associate (CRA) at CBCC Global Research, you will be responsible for on-site monitoring of clinical trials, ensuring compliance with GCP, ICH guidelines, and regulatory processes. You will work closely with cross-functional teams to ensure the success of clinical trials and maintain strong relationships with sites and stakeholders.
Key Responsibilities
Conduct on-site monitoring visits to ensure compliance with GCP, ICH guidelines, and regulatory processes
Review and verify data for accuracy and completeness
Identify and report any issues or concerns to the study team
Collaborate with sites and stakeholders to ensure successful study execution
Maintain accurate and up-to-date study records
Requirements
1-4 years of on-site monitoring experience in clinical trials
Strong understanding of GCP, ICH guidelines, and regulatory processes
Excellent communication and organisational skills
Ability to travel for site monitoring visits
Strong attention to detail and ability to work independently
What CBCC Global Research Offers
Opportunity to work on innovative oncology and non-oncology studies
Collaborative and growth-oriented environment
Competitive compensation and learning opportunities
Professional development and growth opportunities
State-of-the-art facilities and equipment
Why Choose CBCC Global Research?
We are a leading player in the clinical research industry with a strong reputation for excellence
We offer a collaborative and growth-oriented environment that fosters professional development and growth
We provide opportunities for career advancement and learning
We have a strong commitment to quality and compliance
Career Growth and Development
At CBCC Global Research, we’re committed to providing our employees with opportunities for career growth and development. As a CRA, you’ll have the opportunity to work on a wide range of projects and develop your skills in areas such as:
Clinical trial monitoring and management
Regulatory compliance and submissions
Study start-up and close-out
Site management and relationships
Leadership and management
Conclusion
If you’re a highly motivated and experienced CRA looking for a new challenge, we encourage you to apply for this exciting opportunity at CBCC Global Research. With a competitive compensation package, collaborative and growth-oriented environment, and opportunities for professional growth and development, this is a career path you won’t want to miss.
📨 How to Apply
If you’re ready to take your career to the next level, send your updated CV to 📧 sonu.gupta@cbcc.global
We look forward to hearing from you and welcoming you to our dynamic team! 🙌
Frequently Asked Questions
Q: What is the primary responsibility of a Clinical Research Associate (CRA)?
A: The primary responsibility of a CRA is to ensure compliance with GCP, ICH guidelines, and regulatory processes during clinical trials.
Q: What skills are required for a CRA?
A: A CRA should have strong knowledge of GCP, ICH guidelines, and regulatory processes, excellent communication and organisational skills, and the ability to work independently.
Q: What kind of career growth and development opportunities are available?
A: We offer professional development and growth opportunities, including training and certification programs, leadership development, and opportunities to work on high-profile projects.