About the role
The Clinical Research Associate will oversee clinical trial processes, ensuring compliance with regulatory requirements and protocol adherence. Responsibilities include monitoring trial progress, conducting site visits, and collaborating with investigators and study teams. This role is designed for detail-oriented individuals who thrive in a regulatory environment and are passionate about advancing medical research. Our client offers a dynamic work atmosphere and opportunities for professional growth.
What you'll do
- Monitor clinical trial progress.
- Conduct site visits and audits.
- Ensure compliance with regulatory standards.
- Collaborate with study teams and investigators.
What you'll need
- Bachelor's degree in life sciences or related field.
- Experience in clinical trial management.
- Strong understanding of regulatory guidelines.
Skills
Project management.
Effective communication.
Attention to detail.
Good to have
Knowledge of Good Clinical Practice (GCP).
Experience with data management systems.
Benefits
- Competitive salary and benefits.
- Professional development opportunities.
- Supportive 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 main focus of this position?
The focus is on overseeing clinical trial processes and ensuring compliance.
What qualifications are needed?
A degree in life sciences or a related field is required.
Is this position full-time?
Yes, it is a full-time onsite position.
What experience level do I need?
3-7 years of experience in clinical research is preferred.
How can I submit my application?
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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