Job Summary
A company is looking for an Experienced Ophthalmology Clinical Research Associate (CRA) II & Sr. CRAs.
Key Responsibilities
- Monitor all aspects of study sites, including routine monitoring, close-out, and maintenance of study files
- Ensure compliance with informed consent procedures and protocol requirements to protect study patients
- Perform Serious Adverse Event (SAE) reporting and assist in training new employees
Required Qualifications
- University or college degree, or certification in a related allied health profession
- 1 - 3+ years of Clinical Monitoring experience
- Ophthalmology experience is desired
- Ability to work in a fast-paced and constantly changing environment
- Comfortable with technology-based data collection methods
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