About the role
As a Clinical Research Associate, you will be responsible for monitoring clinical trials from initiation to completion. Your duties will involve ensuring that the protocols are followed and that data is collected accurately. You will work closely with clinical teams and collaborate with various stakeholders to ensure the smooth running of studies. This role suits candidates with a keen eye for detail and excellent organizational skills. The team offers a supportive environment focused on professional development and adherence to the highest ethical standards in research.
What you'll do
- Monitor clinical trials and ensure compliance
- Collect and analyze study data
- Collaborate with clinical teams
- Prepare reports for stakeholders
What you'll need
- Bachelor's degree in life sciences
- Experience in clinical research
- Strong communication skills
Skills
Project management
Analytical skills
Attention to detail
Good to have
Knowledge of regulatory guidelines
Experience with data management software
Benefits
- Health insurance
- Professional development opportunities
- Flexible working hours
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 are the primary responsibilities of this role?
You will manage clinical trial processes, monitor compliance, and ensure data accuracy.
What qualifications are required for this position?
A degree in life sciences or related field is preferred.
Is this a remote work opportunity?
No, this position is onsite in Ranchi.
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