About the role
As a Clinical Research Coordinator, you will manage the daily operations of clinical trials, including participant recruitment, data collection, and reporting. You will work closely with research teams and healthcare professionals to ensure adherence to protocols and regulatory standards. This role is suitable for individuals with a solid background in clinical research and excellent organizational skills.
You will be part of a collaborative team that values innovation and quality in research. The position offers a hybrid work model, allowing you to balance remote work with on-site responsibilities, along with competitive compensation and opportunities for career advancement.
What you'll do
- Coordinate and monitor clinical trial activities
- Ensure compliance with ethical and regulatory standards
- Collect and manage data from clinical trials
- Communicate effectively with stakeholders
What you'll need
- Bachelor's or Master's degree in Life Sciences
- 3+ years of experience in clinical research
- Knowledge of GCP and regulatory requirements
Skills
Good to have
Benefits
- Flexible work hours
- Professional development opportunities
- Health benefits
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