Pharmaceutical and device companies need to navigate through many hurdles as they develop drugs, devices and diagnostics that improve and save human life. Pearl Pathways supports companies in their development, manufacturing and marketing of these products.
Pearl Pathways is always looking for talented, dynamic, and customer centric hires. We are currently in expansion mode and are seeking talent for serving on the IRB Board, leading regulatory submission engagements, providing quality compliance support and coordinating clinical research. If you have auditing experience, we are currently seeking GXP auditors with +5 years of FDA, ICH and ISO 13485 experience. Our team is comprised of experts in the fields of drug and device development, medical practice, science, engineering, ethics, quality standards, clinical research, and business and commercialization strategies. If you are up for the challenge of a dynamic and growing company that is in an exciting marketplace and poised for success, Pearl Pathways has the opportunity for you.
Employment or Board Positions
For information regarding employment opportunities or IRB Board positions at Pearl Pathways, send an inquiry or resume to email@example.com.
Current positions open
Regulatory Publication Coordinator. Click here for Job Description.
Clinical Research Associate. Click here for Job Description.
Quality Compliance Advisor. Click here for Job Description.
Regulatory Advisor. Click here for Job Description.
If you have auditing experience, we are currently seeking GXP auditors with +5 years of FDA, ICH and ISO 13485 experience.