Posted in Other 30+ days ago.
OurDocumentProcessorsare responsible for processing clinical study research documentsand prepare them for regulatory review, while utilizing our proprietary software program. This is a production position; speed and accuracy are important to our clients.Over time you will have the opportunityto rotate between various functions and gain new skills and increase your pay!If you're looking for a position where you can contribute using your administrative and database skills, this role might be right for you.This position is internally calledanIRB Operations Specialist.
Why are we hiring?
The clinical research industry is always growing, especially during the COVID pandemic!We are hiring more members to join our operations teams in order to help our clients with their clinical research studies.
Essential Duties/Responsibilities:
What this job is not:
Education Requirements:
Qualifications/Experience
General overview of benefits:
Temporarily Working Remote:
We are currently workingremotely; however, we plan to return to the office environment sometime after July 1st, 2021 or when appropriate to do so. Due to this reason, we are looking for local candidates.
About Us:
For over 50 years, WCG IRB has been at the forefront of protecting the rights and welfare of human subjects during all phases of clinical trials. Recognized as the gold standard of human subject protection, WCG is the trusted partner to over 1,000 institutions in the United States alone, ranging from small community hospitals and research sites to large academic medical centers and universities. Our unparalleled review ensures that human research studies withstand scrutiny around the world.
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