About the role
As a Clinical Trial Associate, you will be responsible for coordinating various aspects of clinical trials, including site management, data collection, and patient recruitment. This role is ideal for individuals with a strong understanding of clinical research and regulatory requirements. You will work closely with clinical research teams to ensure that all trial activities are conducted per applicable guidelines and protocols. Your attention to detail and organizational skills will be essential in maintaining documentation and facilitating communication among stakeholders.
What you'll do
- Coordinate clinical trial activities according to protocols
- Manage communication with study sites and stakeholders
- Ensure compliance with regulatory requirements
- Assist in the preparation of trial documentation
What you'll need
- Bachelor’s degree in life sciences or related field
- At least 2 years of experience in clinical research
- Knowledge of regulatory standards and guidelines
Skills
Strong organizational and communication skills
Proficiency in data management software
Attention to detail and problem-solving abilities
Good to have
Familiarity with Good Clinical Practice (GCP)
Experience with patient recruitment strategies
Benefits
- Competitive salary and performance bonuses
- Opportunity for professional development
- Health and wellness benefits
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
Questions about this job
What are the primary responsibilities of a Clinical Trial Associate?
You will coordinate clinical trials, manage site activities, and ensure compliance with regulatory standards.
What qualifications do I need for this role?
A degree in life sciences or a related field, along with experience in clinical research, is preferred.
Is this position onsite?
Yes, this role requires you to work onsite at our office in SG Highway, Ahmedabad.
Listing last updated