About the role
In this role, you will coordinate various aspects of clinical trials including patient recruitment, data collection, and compliance with regulatory standards. You will be responsible for ensuring the smooth execution of studies while collaborating with investigators and other team members. This role suits individuals with strong organizational skills and a passion for clinical research. Our client offers a supportive environment where you can grow your skills and contribute to meaningful research projects.
What you'll do
- Manage and oversee clinical trial operations
- Ensure compliance with regulatory requirements
- Assist in patient recruitment and retention
- Collect and manage clinical data efficiently
What you'll need
- Bachelor's degree in Life Sciences or similar
- 2-5 years of experience in clinical research
- Knowledge of Good Clinical Practice (GCP)
Skills
Good to have
Benefits
- Competitive salary and benefits package
- Flexible working hours
- Professional development opportunities
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