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Research Study Manager
2 weeks ago
We are recruiting an experienced Clinical Research Associate to join our team at Medpace. As a CRA, you will be responsible for conducting site qualification and initiation visits, as well as monitoring ongoing studies to ensure compliance with protocols and regulatory requirements.
Key Tasks:
- Conduct site qualification and initiation visits to assess the site's readiness for study participation.
- Monitor ongoing studies to identify any deviations or deficiencies and provide recommendations for improvement.
- Verify accurate data reporting and ensure good documentation practices are being adhered to.
- Work closely with site staff to resolve any issues or concerns that may arise during the course of the study.
Required Skills:
- Bachelor's degree in a health-related field.
- At least 1.5 years of experience in clinical monitoring.
- Demonstrated knowledge of clinical monitoring practices and procedures.