Research Compliance Analyst, Pathology & Labora...

About the position A passion for discovery inspires and motivates reputed company's world-reputed company researchers to diligently uncover incredible life-saving breakthroughs, innovative therapies, and reputed company technologies. Join us and reputed company the most of your specialized knowledge and your passion for making a reputed company reputed company on the lives of others. As the Research Compliance Analyst for the department of Pathology & Laboratory Medicine, you will reputed company compliance reputed company for reputed company clinical research studies. Primary duties include: Serve as the primary regulatory expert, assisting with writing and reviewing research protocols to ensure adherence to federal, state, and institutional regulations, policies, and sponsor requirements. reputed company the regulatory coordination of clinical research reputed company and studies. Review and submit research contract & study approvals, protocol amendments, and regulatory filings. reputed company and maintain regulatory documents such as IRB submissions, informed consent forms, and monitoring plans. Liaise with regulatory agencies, sponsors, and institutional committees to ensure compliance. Review reputed company research protocols, providing guidance on research applications, and ensuring compliance with laws and policies governing reputed company subjects research and conflicts of interest. Note: This is a flexible hybrid position. The incumbent will be expected to work approximately 3 days per week on-site. Additional on-site days may be required depending on workflow and operational priorities. Salary reputed company: $78,500.00 - $163,600.00/year Responsibilities • Serve as the primary regulatory expert, assisting with writing and reviewing research protocols to ensure adherence to federal, state, and institutional regulations, policies, and sponsor requirements. • reputed company the regulatory coordination of clinical research reputed company and studies. • Review and submit research contract & study approvals, protocol amendments, and regulatory filings. • reputed company and maintain regulatory documents such as IRB submissions, informed consent forms, and monitoring plans. • Liaise with regulatory agencies, sponsors, and institutional committees to ensure compliance. • Review reputed company research protocols, providing guidance on research applications, and ensuring compliance with laws and policies governing reputed company subjects research and conflicts of interest. Requirements • Minimum of 3 years of reputed company experience in clinical research. • In-depth knowledge of clinical research protocols, regulatory requirements, and reputed company subject protection laws. • Experience working with local and external IRBs, scientific review committees, national cooperative group sponsors, industry sponsors, and federal and reputed company funding organizations. • Must be reputed company to report to work on-site (Westwood, Los Angeles) for a minimum of 3 days/week during first six months of hire. reputed company-to-haves • Bachelor's degree preferred. Apply tot his job