About the role
As a Clinical Trial Assistant, you will assist in the planning and execution of clinical trials. You will be responsible for coordinating with investigators, managing documentation, and ensuring compliance with regulatory requirements. This role is perfect for someone looking to gain experience in the clinical research field while working as part of a dynamic team. You will be supported by experienced professionals who are committed to mentoring and developing your skills in clinical research.
What you'll do
- Assist in the preparation of clinical trial documentation
- Coordinate with investigators and study sites
- Maintain accurate records and databases
- Support regulatory submissions
What you'll need
- Bachelor's degree in Life Sciences or related field
- Knowledge of clinical trial processes
- Strong organizational skills
Skills
Excellent communication skills
Attention to detail
Ability to work in a team
Good to have
Familiarity with clinical trial management systems
Knowledge of Good Clinical Practice (GCP)
Benefits
- Opportunity to work with a leading clinical research team
- Professional development and training
- Competitive salary package
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 a Clinical Trial Assistant?
The primary responsibilities include coordinating clinical trials, managing documentation, and ensuring compliance with regulatory standards.
Is this role suitable for fresh graduates?
Yes, candidates with 1-3 years of experience in clinical research or related fields are encouraged to apply.
What is the work environment like?
The role is onsite in Sector 17, Chandigarh, and involves collaboration with various teams.
Listing last updated