About the role
In the role of Clinical Research Associate, you will be responsible for overseeing clinical trial processes and ensuring they comply with regulatory standards. Your daily tasks will involve monitoring trial sites, coordinating with investigators, and ensuring data integrity. This position is ideal for professionals with a background in clinical research and a passion for advancing medical science.
Our client offers a dynamic work environment with opportunities to work on innovative trials. You will have the chance to collaborate with leading researchers and contribute to impactful healthcare solutions.
What you'll do
- Monitor and manage clinical trials
- Ensure compliance with regulatory requirements
- Coordinate with site investigators and staff
- Review and verify trial data and documentation
- Provide training and support to trial site staff
What you'll need
- Bachelor's degree in life sciences or related field
- 2+ years of experience in clinical research
- Familiarity with GCP guidelines
Skills
Strong organizational skills
Effective communication abilities
Proficiency in data analysis
Good to have
Experience with clinical trial management systems
Knowledge of regulatory affairs
Benefits
- Flexible working hours
- Health benefits and insurance
- Opportunity to work on cutting-edge research
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 does a typical day look like for a CRA?
You will monitor trial sites, review data, and ensure compliance with protocols.
Do I need prior experience in clinical research?
Yes, 2-5 years of experience in a related field is required.
Is this position remote?
This is a hybrid role with both remote and onsite responsibilities.
What is the salary for this role?
The monthly salary ranges from INR 35,000 to INR 60,000.
How can 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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