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CANDIDATES MUST BE WILLING TO COMMUTE TO WESTWOOD, CA (90095)
Day-to-Day
An employer is looking for a Clinical Research Administrator sitting the Westwood Los Angeles area.
This person will be supporting the company’s hematology malignancy clinical trials, ensuring the proper and timely reporting of research data collected on various research studies. 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.
The importance of this position comes from advances in the research study start-up process, increased availability of research trials, and the initiation of remote monitoring activities due to COVID-19. The team is opening new studies and enrolling multiple patients at an impressive rate, and all source documents must be available remotely for sponsor partners.
Must Haves:
- Bachelor’s Degree in related field
- 1+ years of Clinical Research Experience
- Ability to handle a high volume of data/trials at once
- Data management experience (6+ months)
- Experience using any EMR system such as Epic or Medidata (digital version of patients healthcare chart – software programs that allow healthcare practices to create, store, and receive these charts)
Plusses:
- Oncology clinical research background
- GCP Training (Good Clinical Practice)
Benefits and Compensation:
$25-30/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.
