About the role
As a Clinical Research Associate, you will play a key role in designing, implementing, and monitoring clinical trials. Your responsibilities will include compiling data, ensuring compliance with protocols, and liaising with sites and investigators. This position is well-suited for detail-oriented individuals who thrive in a dynamic environment and are passionate about advancing healthcare research. Our flexible hybrid work model allows for a balanced approach to work and life.
What you'll do
- Design and implement clinical trials
- Ensure compliance with regulatory requirements
- Compile and analyze research data
- Communicate with clinical sites and investigators
What you'll need
- Degree in life sciences, pharmacy, or related field
- 2-5 years of experience in clinical research
- Knowledge of GCP and clinical trial regulations
Skills
Strong analytical skills
Excellent communication
Project management skills
Good to have
Experience with data management systems
Knowledge of statistical analysis software
Benefits
- Flexible working hours
- Health benefits
- Opportunities for career advancement
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 does the role entail?
You will oversee clinical trials, ensure regulatory compliance, and compile research data.
What educational background is needed?
A degree in life sciences or pharmacy is preferred.
What is the duration of the contract?
This is a fixed-term contract position with the possibility of extension.
Is travel required for this role?
Yes, some travel to clinical sites may be required.
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