Pearl Pathways is pursuing a Clinical Research Associate to join our team! The CRA will be responsible for the coordination and conduct of clinical research activities either for the sponsor or at a research site. This role will include the day-to-day responsibility for clinical research ensuring studies are conducted in accordance with the protocol, relevant SOPs, and good clinical practices. Pearl Pathways is headquartered in Indianapolis, Indiana with a second office in Houston, Texas. Telecommuting may be an option as well. Please see the full job description and contact information here.
Single IRB – A Guide to the Common Rule sIRB Mandate
The sIRB requirement is active. Is your study affected?
Clinical Research Accelerated
You need high quality, timely board reviews so that you can get your study in the clinic.
Recent Posts
Pearl IRB 2024 Year-End Schedule
Snowball Sampling: Is it ethical to pay your study subjects to recruit participants on your behalf?
Improving Exempt Submissions: 7 Tips to Reduce Revision Requests
Common Rule Exceptions to the Use of a Single IRB for Multi-site Research Ends After May 11, 2023
Pearl IRB 2022 Year-End Schedule