Clinical Research Coordinator
Insight Global
Job Description
An employer is looking for a Clinical Research Coordinator sitting in Westwood CA.
This person will be supporting the company's HIV Trials team, ensuring the proper and timely reporting of research data collected on various research studies as well as other administrative tasks. This includes reporting of research data to the sponsor and to the IRB through their EMR system. This position ensures that the collection and submission of data to sponsoring agencies meet all protocol requirements. This role assists in quality control and quality assurance activities to maintain 'audit-ready' status.
Pay rate: 25-33/hr
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to View email address on click.appcast.io learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:
Skills and Requirements
• Bachelor's Degree in a relevant field
• 2+ years of Clinical Research Coordination experience
• Experience managing clinical research data in a EDC system (such as oncore, recap, medidata)
• Strong patient facing experience managing patient visits
• Ability to work with a sensitive population
• Interventional drug trial experience
• Experience communicating with sponsors
• Knowledge of regulatory practices • Epic experience (source documentation)
• IRB submissions experience
• Academic institution experience because regulations align
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