About the role
In this role, you will manage the day-to-day activities of clinical trials, ensuring compliance with protocols and regulations. You will be responsible for coordinating with study sites, recruiting participants, and collecting and analyzing data. This position is well-suited for someone with a background in clinical research and a strong understanding of medical devices.
Our client values innovation and teamwork, providing a dynamic work environment that encourages professional growth. If you are detail-oriented and passionate about advancing medical science, apply today.
What you'll do
- Manage clinical trial operations
- Recruit and screen participants
- Ensure compliance with regulatory requirements
What you'll need
- Bachelor's degree in life sciences
- 3+ years in clinical research
- Strong knowledge of clinical trial protocols
Skills
Good to have
Benefits
- Flexible working hours
- Opportunity for career advancement
- Collaborative work culture
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