Clinical Research Coordinator

Responsibilities

Looking for a mid-level to Sr. Coordinator that will oversee recruitment, screening, enrollment, scheduling, data collection, participant tracking, and invoicing.

They will also be responsible for study start-up, budget negotiation, IRB submissions, modifications, and amendments, annual renewals, obtaining financial disclosure information from the investigators, preparation for audits and monitor

visits, study closeouts

Required Skills

• 2 years experience as a Clinical Research Coordinator
• Strong understanding of Good Clinical Practice (GCP) and research regulations.
• Excellent communication and organizational skills, with the ability to manage competing priorities.
• Must be comfortable working directly with patients and handling biological samples.
• Must have a valid driver's license and reliable transportation for required sample transport.

Preferred Skills

• Experience in Rheumatology research
• ACRP or SOCRA certified

Schedule/Shift

9am-6pm, M-F

#MedixLS

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.