About the role
In this role, you will be responsible for monitoring clinical trials, ensuring adherence to protocols, and coordinating with research teams. Your expertise will contribute to the successful execution of clinical studies. The position offers a hybrid work environment, allowing flexibility while ensuring you stay connected with your team. If you are detail-oriented and passionate about advancing medical research, we want to hear from you.
What you'll do
- Monitor clinical trial activities and site performance
- Ensure compliance with regulatory requirements
- Prepare study-related documentation
- Communicate with investigators and stakeholders
What you'll need
- Bachelor's degree in life sciences or related field
- 3-6 years of experience in clinical research
- Knowledge of GCP and regulatory guidelines
Skills
Strong analytical skills
Excellent communication abilities
Ability to work under pressure
Good to have
Familiarity with data management systems
Project management skills
Benefits
- Contractual engagement with competitive pay
- Flexible working hours
- Opportunity to work on innovative research projects
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 daily responsibilities of a Clinical Research Associate?
You will monitor clinical trials, prepare reports, and liaise with research teams and regulatory bodies.
Is this role remote or onsite?
This is a hybrid role, combining both onsite and remote work.
What qualifications do I need?
A degree in life sciences is required, along with 3-6 years of relevant experience.
How do I apply for this job?
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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