About the role
As a Clinical Research Associate, you will play a vital role in overseeing clinical trials and ensuring compliance with regulatory standards. You will collaborate with various stakeholders to monitor study progress, collect data, and maintain accurate documentation.
Key responsibilities include site management, patient recruitment, and ensuring adherence to protocols. You will also conduct site visits and assist in training site staff, fostering a collaborative environment for successful trial execution.
Our client offers a supportive work culture and opportunities for professional growth in the dynamic field of clinical research. This role is ideal for individuals with strong organizational skills and a passion for advancing medical knowledge.
What you'll do
- Monitor clinical trial sites
- Ensure compliance with regulations
- Coordinate with investigators
- Manage clinical trial documentation
What you'll need
- Degree in Life Sciences
- 2-5 years of experience in clinical research
- Strong organizational skills
Skills
Good to have
Benefits
- Competitive salary
- Hybrid work model
- Professional development opportunities
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