About the role
As a Clinical Research Associate, you will play a crucial role in monitoring clinical trials and ensuring compliance with established protocols and regulatory standards. Your responsibilities will include liaising effectively between the sponsor and site staff, facilitating timely recruitment, and ensuring adherence to project timelines.
This position is ideal for detail-oriented professionals who have a passion for clinical research and thrive in a fast-paced environment. The hiring company offers a hybrid work model, providing flexibility while maintaining high standards of quality in research. Join a dedicated team that values innovation and integrity in advancing medical science.
What you'll do
- Monitor and manage clinical trial sites.
- Ensure compliance with regulatory requirements.
- Prepare and review study documentation.
- Facilitate communication between sites and sponsors.
- Report on trial progress and issues.
What you'll need
- Bachelor's degree in life sciences or a related field.
- Experience in clinical research or monitoring.
- Familiarity with GCP and regulatory guidelines.
Skills
Good to have
Benefits
- Attractive salary with performance incentives.
- Flexible work environment with a hybrid model.
- Access to ongoing training and development.
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