About the role
As a Clinical Research Associate, you will be instrumental in managing clinical trials from initiation through completion. Your responsibilities will include monitoring trial progress, ensuring data integrity, and maintaining communication with study participants and investigators. This role is suitable for individuals with a strong background in clinical research and a passion for advancing medical knowledge. You will work closely with various stakeholders to guarantee that all trials adhere to regulatory standards and ethical practices. Join a dedicated team committed to improving patient outcomes through innovative research.
What you'll do
- Monitor clinical trial progress and ensure compliance.
- Communicate with stakeholders and provide updates.
- Prepare and maintain study documentation and reports.
- Assist in training site staff on study protocols.
What you'll need
- Degree in life sciences or related field.
- Experience in clinical research monitoring.
- Strong understanding of GCP and regulatory requirements.
Skills
Excellent communication skills.
Strong analytical and problem-solving abilities.
Detail-oriented with strong organizational skills.
Good to have
Knowledge of statistical analysis software.
Experience with electronic data capture systems.
Benefits
- Competitive salary with performance bonuses.
- Opportunities for professional development.
- Supportive team environment.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
Clinical Research Associate jobs in other cities
Questions about this job
What qualifications are needed for this role?
A degree in life sciences or a related field is required, along with experience in clinical research.
Where will the role be based?
The position is based in Gwalior, specifically in the Civil Lines area.
What is the typical duration of the contract?
The contract is typically for a period of 12 months with the possibility of extension.
Listing last updated