About the role
In this role, you will oversee clinical trials, ensuring compliance with regulatory standards and protocols. Your day-to-day tasks will involve monitoring study sites, collecting data, and collaborating closely with investigators. This position is ideal for professionals with a passion for advancing healthcare through research and a strong attention to detail. Our client offers a supportive environment for career growth and skill development.
What you'll do
- Oversee clinical trials and study sites
- Maintain compliance with regulatory guidelines
- Collect and analyze clinical data
- Collaborate with investigators and site staff
What you'll need
- Bachelor's degree in life sciences
- 2-5 years of experience in clinical research
- Strong understanding of regulatory requirements
Skills
Attention to detail
Strong communication skills
Analytical thinking
Good to have
Project management
Statistical analysis
Benefits
- Career growth opportunities
- Health insurance
- Flexible working hours
Interested in this role?
It takes about two minutes. Free to apply — NodHire never asks candidates for money.
Questions about this job
What are the primary responsibilities of a Clinical Research Associate?
You will monitor clinical trials, ensure compliance with regulations, and collect and analyze data.
What qualifications are needed for this role?
A bachelor's degree in life sciences and prior experience in clinical research are essential.
What is the work mode for this position?
This is an onsite position based in Whitefield, Bengaluru.
What is the expected salary range?
The salary range for this role is between INR 60,000 to INR 80,000 per month.
Listing last updated