About the role
In the Clinical Research Coordinator role, you will oversee the planning and execution of clinical trials. You will be responsible for participant recruitment, data collection, and ensuring that the research adheres to ethical standards and regulatory guidelines. The ideal candidate will have a strong background in clinical research and excellent organizational skills.
You will collaborate with various stakeholders, including researchers and healthcare professionals, to ensure successful project outcomes. This position offers the flexibility of hybrid work, allowing you to balance onsite responsibilities with remote tasks. If you are looking for a challenging opportunity to advance your career in clinical research, we encourage you to apply.
What you'll do
- Manage all aspects of clinical trials from start to finish
- Recruit and screen study participants
- Ensure compliance with regulatory requirements and ethical standards
- Collect and manage study data accurately
What you'll need
- Bachelor's degree in life sciences or related field
- 3-6 years of experience in clinical research
- Strong knowledge of GCP and regulatory guidelines
Skills
Good to have
Benefits
- Competitive salary and benefits package
- Opportunity to work on cutting-edge research
- Flexible work environment
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