About the role
As a Clinical Research Associate, you will manage and monitor clinical trials, ensuring compliance with regulatory standards and protocols. Your responsibilities will include coordinating with study sites, managing trial documentation, and conducting site visits to ensure data integrity. This role requires excellent organizational skills and the ability to work collaboratively within a team. Our client offers a dynamic work environment with opportunities to contribute to groundbreaking research in healthcare.
What you'll do
- Oversee and monitor clinical trials.
- Ensure compliance with regulatory guidelines.
- Coordinate with study sites and manage documentation.
- Conduct site visits and prepare reports.
What you'll need
- Degree in Life Sciences or related field.
- Experience in clinical research management.
- Strong analytical and problem-solving skills.
Skills
Strong understanding of clinical trial protocols.
Excellent communication and organizational skills.
Ability to work independently and in a team.
Good to have
Familiarity with clinical trial management software.
Experience in patient recruitment and retention.
Benefits
- Opportunity to work on innovative research projects.
- Competitive salary and benefits.
- Flexible work arrangements.
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 the key responsibilities of a Clinical Research Associate?
You will manage clinical trials, ensure compliance, and conduct site visits.
What qualifications are needed for this role?
A degree in Life Sciences or a related field and prior experience in clinical research are required.
Is this a temporary position?
Yes, this is a temporary hybrid role.
What is the salary range for this position?
The salary ranges from INR 50,000 to INR 80,000 monthly.
How do I apply for this job?
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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