About the role
In this position, you will coordinate clinical trial activities, manage timelines, and ensure compliance with regulatory standards. Your responsibilities will include liaising with stakeholders, preparing reports, and ensuring that all trial protocols are followed accurately. This role suits someone with strong project management skills and a background in clinical research. You will work closely with healthcare professionals and researchers to contribute to groundbreaking medical advancements.
What you'll do
- Coordinate all phases of clinical trials.
- Ensure compliance with regulatory requirements.
- Communicate with stakeholders and prepare documentation.
- Monitor trial progress and report findings.
What you'll need
- Bachelor's degree in Life Sciences or a related field.
- Experience in clinical trial management.
- Strong organizational and communication skills.
Skills
Project management.
Knowledge of clinical trial regulations.
Excellent communication skills.
Good to have
Experience with data management software.
Familiarity with electronic data capture systems.
Benefits
- Flexible working hours.
- Professional development opportunities.
- Collaborative work environment.
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 is the duration of the contract?
The contract is for a period of one year, with the possibility of extension.
Is remote work an option?
Yes, this role allows for a hybrid work model.
What qualifications do I need?
A degree in Life Sciences or related field, along with experience in clinical research.
What is the salary for this position?
The salary ranges from INR 60,000 to INR 80,000 per month.
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