About the role
In this role, you will be responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and maintaining study documentation. As a Clinical Research Associate, you will collaborate with cross-functional teams to support the successful execution of clinical studies. This position suits detail-oriented professionals looking to impact healthcare through research.
We offer flexible working arrangements and a dynamic environment that encourages career growth. If you are passionate about clinical research and patient safety, this is the perfect opportunity for you.
What you'll do
- Monitor clinical trials and ensure compliance.
- Collaborate with study teams to facilitate research.
- Maintain accurate study documentation.
- Communicate with stakeholders regarding trial progress.
What you'll need
- Bachelor's degree in life sciences.
- 2+ years of experience in clinical research.
- Familiarity with regulatory requirements.
Skills
Strong analytical skills.
Excellent communication skills.
Detail-oriented approach.
Good to have
Knowledge of GCP guidelines.
Experience with data management systems.
Benefits
- Flexible working hours.
- Opportunity to work on cutting-edge research.
- Professional development support.
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 is the main role of a Clinical Research Associate?
The Clinical Research Associate monitors clinical trials, ensuring compliance and maintaining documentation.
Is this a remote position?
Yes, this role is fully remote.
What qualifications do I need for this role?
A degree in life sciences and 2+ years of experience in clinical research is required.
What is the salary range for this position?
The salary ranges from INR 40,000 to INR 70,000 monthly.
How do I apply for this position?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
Listing last updated