About the role
In this role, you will oversee clinical trials from initiation through to completion, ensuring compliance with regulatory requirements and protocols. You will collaborate with various stakeholders, including clinical sites and monitors, to facilitate the successful execution of clinical studies. The ideal candidate will possess strong organizational skills and a thorough understanding of clinical research methodologies. The team values initiative and offers a dynamic working environment with opportunities for advancement.
What you'll do
- Coordinate and manage clinical trials.
- Ensure compliance with regulations and protocols.
- Monitor trial progress and collect data.
- Communicate with investigators and stakeholders.
What you'll need
- Bachelor's degree in life sciences or related field.
- 3-5 years of experience in clinical research.
- Familiarity with clinical trial regulations.
Skills
Strong analytical and problem-solving skills.
Excellent communication and interpersonal skills.
Detail-oriented and organized.
Good to have
Experience with clinical trial management software.
Knowledge of Good Clinical Practice (GCP) guidelines.
Benefits
- Flexible work schedule.
- Opportunities for career growth.
- Exposure to cutting-edge research.
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 the role of a Clinical Research Associate involve?
You will manage clinical trials, ensure compliance, and liaise with various stakeholders.
What qualifications are required?
A degree in life sciences or related field, along with experience in clinical research.
Is this position remote or onsite?
This is a hybrid role, allowing for both remote and onsite work.
What is the salary for this position?
The salary ranges from INR 60,000 to INR 80,000 monthly.
How can 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.
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