Principal Trainer, Clinical Education
Lead onboarding, training development, and competency programs for clinical operations across multi-site teams.
Remote • Panamá Province, Panama
- Full Time
- $140,000 – $220,000
- Min. 4 YOE
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Lead onboarding, training development, and competency programs for clinical operations across multi-site teams.
Coordinate and monitor clinical studies ensuring regulatory compliance and patient safety.
Execute CTMS site and study builds, QC checks, and operational reporting to enable final build acceptance.
Lead GxP quality programs for SaaS products, including AI, across the software lifecycle.
Lead study start-up activities, coordinating cross-functional teams to activate sites and ensure timely activation.
Support participant care and event operations, including phlebotomy, specimen handling, and documentation.
Lead end-to-end live events and film productions, coordinating timelines, budgets, vendors, and on-site operations.
Coordination of retention activities for participants in Future of Medicine program, delivering education and virtual engagement to optimize enrollment and study participation.
Leads recruitment partner ecosystem, contracts and ensures performance to accelerate enrollment across trials.
Coordinate clinical research activities ensuring protocol compliance and patient management across trials.
Provide regional travel and remote tele-medicine support for clinical studies, administering varied investigational products.
Leads LATAM site support operations, hires and trains staff, and partners with sponsor teams to drive study results.
Coordinate and monitor clinical trials per GCPs, ensuring regulatory compliance and patient care across study activities.
Lead end-to-end Clinical Delivery projects, manage scope, budget, and client satisfaction to drive successful outcomes in remote/spanning clinical trials.
Oversee development, negotiation, and execution of contracts for research services in a remote U.S. role.
Coordinating travel-based clinical trials, ensures GCP compliance while enrolling and monitoring subjects.
Lead site operations for a clinical research site, directing staff and ensuring regulatory compliance and study execution.
Design, build and maintain data pipelines, data marts, and other data components needed for the data analytics team.
Fosters strong community relationships to support health initiatives and execute community events and campaigns.
Provide frontline technical and product support to Care Access staff, troubleshooting issues and guiding users through systems and processes.
Leads IT operations and infrastructure in a healthcare environment, balancing strategic roadmaps with hands-on execution.
Provide phlebotomy and biospecimen handling at mobile clinical research events, ensuring compliance and participant comfort.
Support clinical research events with phlebotomy, specimen handling, data management, and patient care.
Provide strategic and practical legal advice on global privacy and data protection laws, including GDPR, HIPAA, CCPA/CPRA, and other U.S. privacy laws.