Clinical Research Document Processors

Description and Requirements

Our Clinical Study Document Processors are responsible for processing clinical study research documents 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 opportunity to 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 called IRB 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

• The primary responsibility will be to collect, revise, and process clinical trial and protocol documents in preparation for our board’s review.
• Review and edit the documents to comply with company formatting standards.
• Enter data into our proprietary software.
• Work effectively in a queue with high volumes and frequent changes, all while meeting rigid deadlines.
• Maintain both speed and accuracy requirements.
• Overtime is often required in order to meet deadlines and to help clinical trial participants.  We estimate 0-10 hours of overtime weekly, depending on company needs.

What this job is not:

We are not editors. Our review process is focused on the content of the clinical study, which is submitted to us by our clients.

Education Requirements:

• HS Diploma is required
• College Graduates are encouraged to apply.

Qualifications/Experience:

• Bachelor’s degree or two+ years of office experience where proofing documents and attention to detail were essential elements of your job requirements.
• Intermediate skills with Microsoft Word and Microsoft Outlook.
• A background in utilizing specialized database systems to process work is strongly desired.
• Ability to quickly proofread and detect errors in formatting.

Our Benefits

• Competitive salary
• Robust medical, dental and vision plans – within 30 days of your employment.
• 20 PTO days to start and 11 paid holidays annually
• Matching 401K program
• No parking fees
• Tuition reimbursement
• More!!!

Remote:  

We are currently working remotely; however, we plan to return to the office environment when it’s appropriate to do so.  Due to this reason, we are looking for local candidates.

About Us

For over 50 years, Western Institutional Review Board® (WIRB), a member of the WIRB-Copernicus Group (WCG,) 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, WIRB is the trusted partner to over 1,000 institutions in the United States alone.  Our team members are passionate about growth, innovation and collaboration. We are constantly striving to impact the healthcare needs today and in the future!  If you wish to be a part of a company which is making a difference around the globe, apply today!

WCG is proud to be an equal opportunity employer – Qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, sexual orientation, gender identity, age, marital status, disability, veteran status or any other status protected by law.