About the role
As a Clinical Research Associate, you will be responsible for monitoring and coordinating clinical trials from initiation to completion. Your key responsibilities will include site selection, initiation, and ongoing management, as well as ensuring adherence to protocols and regulatory requirements. This role is ideal for individuals who are detail-oriented and passionate about advancing medical research. You will work with a dynamic team, contributing to innovative projects that make a difference in healthcare.
What you'll do
- Monitor clinical trials and ensure compliance with protocols
- Conduct site evaluations and maintain site relations
- Prepare and review study documentation
- Assist in training site staff on study protocols
What you'll need
- Bachelor's degree in life sciences or related field
- 2-5 years of experience in clinical research
- Strong understanding of regulatory requirements
Skills
Excellent communication skills
Detail-oriented with strong organizational skills
Ability to work independently and as part of a team
Good to have
Experience with electronic data capture systems
Knowledge of Good Clinical Practice (GCP)
Benefits
- Competitive salary
- Opportunity to work on innovative clinical trials
- Professional development and training opportunities
Interested in this role?
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Questions about this job
What are the primary responsibilities of this role?
The Clinical Research Associate monitors clinical trials, ensures compliance with protocols, and maintains communication with sites.
What qualifications are required?
Candidates should have a degree in life sciences and relevant experience in clinical research.
Is this an onsite position?
Yes, this role is onsite at the Durgapur Steel Plant.
What is the salary range for this position?
The salary range is between INR 40,000 to INR 80,000 monthly.
How can I apply for this position?
Click "Apply Now" on this page to apply through Hi5 Jobs. Hi5 Jobs is recruiting for this role on behalf of a client employer.
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