Clinical Trials Coordinator Continuing Education Form

Track Your Clinical Research Continuing Education with Ease

Clinical trials coordinators operate in one of the most regulated and rapidly evolving fields in healthcare. Maintaining current certifications, staying updated on IRB compliance requirements, and documenting continuing education units (CEUs) isn't just professional development—it's essential for patient safety, regulatory compliance, and career advancement.

This Clinical Trials Coordinator Continuing Education Form provides a structured way to log completed training, track CEU credits toward certification renewal, document IRB compliance updates, and record best practices in informed consent procedures. Whether you're managing your own professional development or overseeing a team of clinical research professionals, this template helps you maintain accurate records that satisfy regulatory bodies, certification organizations, and institutional requirements.

Designed for Clinical Research Professionals

This form template is built specifically for clinical trials coordinators, clinical research coordinators (CRCs), principal investigators, research nurses, and regulatory affairs professionals who need to:

• Track CEU credits toward certifications like CCRC, CCRP, ACRP, or SOCRA requirements
• Document IRB compliance training including GCP, ICH guidelines, and institutional updates
• Record informed consent training and best practice updates for participant protection
• Plan certification renewals with clear visibility into credit requirements and deadlines
• Maintain audit-ready records that demonstrate ongoing professional competency

The form captures all essential details including training provider information, contact hours, certification body requirements, and compliance topics covered—creating a comprehensive professional development portfolio.

Streamline Compliance Documentation

Clinical research organizations, academic medical centers, and contract research organizations (CROs) can use this form to standardize how their teams report and track continuing education. When combined with Stepper, Paperform's AI-native workflow builder, you can automatically route completed forms to department heads for review, update team training matrices, send reminder emails for upcoming certification deadlines, and maintain centralized records across multiple sites or studies.

For organizations that require verification and signatures on training records, Papersign makes it simple to convert form submissions into official training certificates or acknowledgment documents that coordinators and supervisors can sign electronically—keeping everything audit-ready and compliant.

Why Paperform for Clinical Research Training

Paperform's professional form builder gives clinical research teams the flexibility to create forms that match institutional branding while capturing complex training data with conditional logic and calculations. Track multiple certification pathways, automatically calculate total CEU credits earned, and route different training types to appropriate department reviewers—all within one platform.

With SOC 2 Type II compliance, secure data handling, and integration capabilities with learning management systems, HRIS platforms, and research documentation tools, Paperform provides the security and connectivity that clinical research organizations require. Start with this template and customize it to match your institution's specific certification requirements, training categories, and documentation standards.