About the role
In this role, you will be responsible for managing clinical trials and ensuring compliance with protocols. Daily tasks include liaising with clinical sites, monitoring patient recruitment, and reviewing data integrity. This position suits detail-oriented individuals with a passion for improving patient outcomes through research. You will work within a collaborative team dedicated to advancing medical knowledge.
Your experience in clinical research will be crucial as you handle documentation, train site staff, and communicate findings to stakeholders. The role offers an opportunity to grow in a dynamic environment where your contributions will directly impact clinical practices. Join us in making a difference in healthcare.
What you'll do
- Manage and monitor clinical trial activities.
- Ensure compliance with clinical trial protocols.
- Liaise with clinical sites and stakeholders.
- Train and support site staff on study protocols.
- Review and validate data collected during trials.
What you'll need
- Bachelor's degree in Life Sciences or related field.
- Minimum 2 years of experience in clinical research.
- Knowledge of regulatory requirements and Good Clinical Practice.
Skills
Good to have
Benefits
- Competitive salary.
- Opportunity for professional growth.
- Collaborative work environment.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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