|Title:||Part-time Regulatory Document Specialist|
|Job Status:||Part-time, Benefited|
This position works with our internal teams to ensure the accuracy and completeness of highly-detailed regulatory documents related to our clinic studies. The Specialist tracks completeness, performs archival and quality checks, maintains the various documentation logs and study correspondence, and generally acts as a liaison between Study Managers, IRB Representatives, Admissions, Principal Investigators and Project Managers.
We seek an extremely detail-orientated and process-flow minded candidate. If your heart races when you are reviewing documents for completeness and errors or you are at your happiest when mapping a project timeline balancing the needs of various stakeholders, then you may just be the candidate we seek!
Associate degree in life sciences or related area required; advanced studies preferred.
Clinical research industry experience or training in regulatory arena preferred.
Strongly prefer experience with IRB/FDA and/or other regulatory bodies and guideline compliance.
Strong organizational ability, attention to detail, multi-tasking success, and time management skills.
Excellent oral and written communication skills.
Please note: This position is anticipated to work 30 hours/week during regular business hours, Monday-Friday.