About the role
As a Clinical Research Associate, you will be responsible for monitoring clinical trials from start to finish. This includes site selection, initiation, monitoring, and closeout. You will ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and the protocol. This role is suitable for individuals with strong analytical skills and a passion for advancing medical research. You will work collaboratively with various stakeholders to ensure successful trial outcomes and contribute to innovative healthcare solutions.
What you'll do
- Monitor clinical trial sites
- Ensure compliance with GCP and regulatory standards
- Assist in data collection and reporting
- Collaborate with cross-functional teams
What you'll need
- Degree in Life Sciences
- Experience in clinical research
- Knowledge of regulatory requirements
Skills
Strong analytical skills
Attention to detail
Excellent communication skills
Good to have
Familiarity with clinical trial software
Experience in project management
Benefits
- Attractive salary
- Flexible working hours
- Professional development opportunities
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 will my daily responsibilities include?
Daily responsibilities include monitoring clinical trial sites, ensuring compliance, and assisting in data collection.
What qualifications are needed for this role?
A degree in life sciences and experience in clinical research are required.
Is this position hybrid?
Yes, this is a hybrid role with both remote and onsite responsibilities.
What is the salary range for this role?
The salary ranges from INR 60,000 to INR 100,000 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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