About the role
In this role, you will oversee the design, implementation, and monitoring of clinical trials. Your responsibilities include managing study protocols, ensuring compliance with regulatory standards, and liaising between researchers and participants. The ideal candidate will have a strong understanding of clinical research methodology and excellent organizational skills.
You will work closely with healthcare professionals and researchers, contributing to groundbreaking studies that enhance patient care. Joining our client means being part of a team dedicated to advancing medical knowledge and improving lives.
What you'll do
- Manage clinical trial protocols
- Ensure compliance with regulatory requirements
- Coordinate communication between researchers and participants
- Monitor trial progress and data integrity
What you'll need
- Bachelor's degree in a related field
- Experience in clinical research
- Strong attention to detail
Skills
Project management
Data analysis
Regulatory knowledge
Good to have
Multilingual proficiency
Clinical data management
Benefits
- Health insurance
- Paid time off
- Career advancement 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 qualifications do I need for this role?
A degree in life sciences, nursing, or a related field is required.
Is this position onsite?
Yes, this position is onsite in Nashik.
What is the salary range for this role?
The salary ranges from INR 50,000 to INR 90,000 monthly.
What are the key responsibilities?
You'll oversee clinical trial operations, manage protocols, and ensure compliance.
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