Clinical Research Assistant

Conducts safe and appropriate aseptic and sterile field techniques Assist Coordinator in monitoring subject flow and assist in subject care and management Observe, assist, collect, and record all necessary data for follow up Ensure that treatment room is fully stocked with ancillary supplies ahead of each day Explain treatment processes and procedures to study subjects Set up, prepare subject, and assist in administration of treatment on subjects as required per study protocol and pharmacy/procedure manual Perform post-treatment procedures Document post-injection evaluation per protocol by treating investigator Monitor on-site temperature for all equipment and document daily logs (if applicable)

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA). This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.