**Candidate's must be on-site in Westwood, CA three days a week**
**Candidate's must have experience within Regulatory**
Job Description:
An employer is looking for a Regulatory Coordinator sitting in the Westwood Los Angeles area. This individual will be supporting the regulatory functions within their Rheumatology clinical trials division. They will be supporting 10 PIs and the Clinical Research Supervisor with additional administration functions. This individual will be gathering documents for IRB submissions. This person will not be in a patient facing role.
Must Haves:
- Bachelors Degree
- 1+ years of experience within clinical research
- 1+ year of experience within regulatory - or basic knowledge of Regulatory (know how to read study protocols)
- Strong administrative support within a clinical research setting
- Any EMR software experience (Epic)
-Strong communication, work ethic, and
Plusses:
-Experience working with an IRB System: institution review board
- Working knowledge of financial disclosures, 1572s, and inform consent documents
Compensation:
$25 to $32/hour
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.