ProPharma Group is seeking a Central Monitoring Associate to support clinical monitoring teams using centralized data and SOP-driven processes. The role emphasizes regulatory compliance, ICH GCP guidelines, and quality standards throughout the study lifecycle.
Ideal candidates will have 3+ years in study coordination or in-house monitoring within biotech/pharma and experience with EDC/CTMS systems. The position offers remote work with hybrid collaboration and adherence to SOPs and project plans.
#J-18808-LjbffrRemote Senior Central Monitoring Specialist in raleigh at Unknown Company
This position is listed as full time and able to be worked remotely.