About the role
In this role, you will manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements. You will be responsible for monitoring trial sites, collecting data, and collaborating with cross-functional teams to achieve study objectives. This position is suitable for professionals with a background in clinical research and a passion for advancing healthcare. The hybrid work model allows flexibility while ensuring adherence to project timelines. Our client offers a dynamic environment that fosters innovation and collaboration.
What you'll do
- Oversee clinical trial sites and monitor compliance
- Collect and analyze trial data
- Collaborate with clinical teams and stakeholders
- Prepare reports and documentation for regulatory submissions
What you'll need
- Bachelor's degree in Life Sciences or related field
- 3+ years of experience in clinical research
- Familiarity with GCP and regulatory requirements
Skills
Strong communication skills
Project management capabilities
Analytical thinking
Good to have
Familiarity with clinical trial management software
Certification as a Clinical Research Associate
Benefits
- Flexible work hours
- Health and wellness programs
- 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 does a Clinical Research Associate do?
They manage clinical trials, ensuring compliance and data integrity throughout the process.
Is this position hybrid or fully remote?
This is a hybrid position, requiring both remote work and onsite visits.
What experience is needed for this role?
Candidates should have at least 3 years of experience in clinical research.
What is the salary for this position?
The salary ranges from INR 45,000 to INR 70,000 per month.
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.
Listing last updated