About the role
In this role, you will coordinate all aspects of clinical trials, from participant recruitment to data collection and reporting. You will work closely with research teams and ensure that studies are conducted efficiently and ethically. This position is ideal for those with strong organizational skills and a passion for advancing medical research.
You will be responsible for maintaining regulatory compliance, training study staff, and facilitating communication between stakeholders. Our team fosters a supportive environment where you can grow your career in clinical research and contribute to innovative healthcare solutions.
What you'll do
- Coordinate all phases of clinical trials.
- Ensure compliance with regulatory standards.
- Maintain study documentation and data integrity.
- Train and supervise study staff.
- Facilitate communication between stakeholders.
What you'll need
- Bachelor's degree in life sciences or related field.
- 2-5 years of experience in clinical research.
- Knowledge of regulatory requirements for clinical trials.
Skills
Good to have
Benefits
- Competitive salary and benefits package.
- Opportunities for professional development.
- Supportive work environment.
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