Clinical Research Associate
$75,480–$94,350 year
On-siteNew York, United States or New Jersey, United States
Job Summary
Coordinate all activities for setting up and monitoring clinical trials, including Ophthalmology and multi-TA studies, while completing accurate status reports and maintaining documentation. Run sponsor-generated queries efficiently, manage study cost efficiency, and participate in feasibility studies for new proposals. Develop strong relationships with stakeholders, clinical investigators, and site staff to ensure compliance with protocols and regulatory requirements. Requires a university degree in medicine or science, knowledge of ICH-GCP guidelines, and approximately 60% travel. Salary range $75,480-$94,350.
Required Qualifications
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
- Experience monitoring Ophthalmology trials or multi-TA
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