About the role
As a Clinical Research Associate, you will manage and monitor clinical trials, ensuring compliance with protocols and regulatory requirements. Your responsibilities will include site selection and initiation, monitoring patient safety, and maintaining study documentation. You will collaborate with investigators and the project management team to achieve study objectives.
This role suits professionals passionate about advancing medical research and improving patient outcomes. You will benefit from a supportive work environment and opportunities for professional development through various training programs.
What you'll do
- Manage clinical trials
- Monitor compliance with protocols
- Ensure patient safety
- Maintain study documentation
What you'll need
- Degree in life sciences
- 3-6 years of experience in clinical research
- Understanding of regulatory standards
Skills
Project management
Attention to detail
Communication skills
Good to have
Statistical analysis
Knowledge of clinical trial software
Benefits
- Competitive salary
- Professional development
- Supportive work environment
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What are my key responsibilities?
You will manage clinical trials, monitor compliance, and ensure patient safety.
What qualifications do I need?
A degree in life sciences and experience in clinical research management are required.
Is there flexibility in work arrangements?
Yes, this is a hybrid role with both onsite and remote work options.
What is the salary for this position?
The salary is between INR 50,000 and INR 80,000 monthly.
How do I apply?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
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