About the role
As a Clinical Research Coordinator, you will manage the operational aspects of clinical trials, ensuring that they are conducted according to regulatory requirements and study protocols. You will be responsible for participant recruitment, data collection, and maintaining study documentation. This role is ideal for someone who is detail-oriented and passionate about advancing medical research.
You will work closely with investigators, sponsors, and other team members to facilitate the smooth running of trials. Your role includes preparing reports, monitoring patient progress, and ensuring the integrity of the data collected. This contract position offers flexibility with a hybrid work model, providing an excellent opportunity for those seeking work-life balance while contributing to impactful research.
What you'll do
- Oversee the operational aspects of clinical trials
- Recruit and manage study participants
- Ensure compliance with regulatory standards
- Prepare study documentation and reports
- Monitor data collection and integrity
What you'll need
- Bachelor's degree in life sciences or related field
- 3-6 years of experience in clinical research
- Strong understanding of regulatory requirements
Skills
Good to have
Benefits
- Flexible hybrid work model
- Competitive salary
- Opportunity to work on impactful research projects
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