About the role
As a Clinical Research Associate (CRA), you will monitor clinical trials and ensure compliance with regulatory standards. Your role will involve coordinating with investigators, collecting data, and analyzing trial results. This part-time position is ideal for professionals who wish to balance work and personal commitments while contributing to vital research.
The ideal candidate will possess strong organizational skills and a keen attention to detail. You will be part of a supportive team that values collaboration and innovation in clinical research.
What you'll do
- Monitor clinical trials and ensure compliance.
- Coordinate with trial participants and investigators.
- Collect and analyze trial data.
- Prepare reports and documentation.
What you'll need
- Bachelor's degree in life sciences or related field
- Experience in clinical research
- Familiarity with regulatory compliance
Skills
Strong analytical skills
Excellent communication skills
Attention to detail
Good to have
Knowledge of clinical trial regulations
Experience with data management systems
Benefits
- Flexible work arrangements
- Possibility of transitioning to a full-time role
- Access to training and development
Interested in this role?
It takes about two minutes. Free to apply — Hi5 Jobs never asks candidates for money.
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Questions about this job
What is the expected work schedule for this part-time role?
You will have a flexible schedule, working on average 20 hours a week.
What qualifications are required for this position?
Candidates should have a degree in life sciences and experience in clinical research.
How can I advance in this role?
There are opportunities for further training and advancement within clinical research.
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