About the role
In the role of Clinical Research Associate, you will monitor clinical trials and ensure compliance with regulatory requirements. You will be responsible for managing trial sites, coordinating with investigators, and ensuring the collection of accurate data. This position is well-suited to individuals with strong organizational skills and a passion for clinical research.
Our client offers a flexible part-time arrangement that allows for remote work, making it an ideal opportunity for professionals seeking work-life balance while contributing to meaningful healthcare advancements.
What you'll do
- Monitor clinical trial sites for regulatory compliance.
- Coordinate with clinical investigators and study staff.
- Review data for accuracy and completeness.
- Report findings and address issues as they arise.
What you'll need
- Bachelor's degree in Life Sciences or related field.
- Experience in monitoring clinical trials.
- Knowledge of GCP regulations.
Skills
Good to have
Benefits
- Competitive compensation.
- Flexible working hours.
- Opportunities for professional development.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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