CLINICAL RESEARCH
PROFESSIONAL ESSENTIALS
Anna Nagel
2026 Design and Management of
Cancer Clinical Trials Course
Distributed by:
AN

Issued to

Anna Nagel

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Credential Verification

Issue date: September 29, 2026

ID: f1f71aef-dcf3-4c29-9fb7-b873f799cde6

Sylvester Comprehensive Cancer Center logo

Issued by

Sylvester Comprehensive Cancer Center

The University of Miami Sylvester Comprehensive Cancer Center is the only National Cancer Institute-designated cancer center in South Florida and is known as South Florida’s leader in patient-focused cancer research and care.

Type

Course

Format

Online

Description

The Sylvester Design and Management of Cancer Clinical Trials Course provides key information to advance translational clinical research, foster better clinical trial design, and ultimately improve patient care. Clinical research education works best when people learn together—not in silos. This course brings the full research team together, including PIs, advanced practice providers, nurses, clinical research coordinators, regulatory and lab staff, other clinical research professionals, PhD scientists, and trainees at all levels. Participants gain a strong foundation in cancer clinical research, and by learning in a shared virtual environment, attendees build common understanding, strengthen teamwork, and become better equipped to collaborate for clinical trial success. Holders of this badge engaged with topics that are essential for clinical research professionals: how to collaborate with other members of the research team for clinical trial success; fundamentals of valid, informed consent; and regulatory submissions and IRB processes.

Skills

Clinical Research

Informed Consent

Regulatory Process

Cancer Clinical Trials

Collaboration

Earning Criteria

Participation

Attended lectures and panels discussions about topics that are essential for clinical research professionals: how to collaborate with other members of the research team for clinical trial success; fundamentals of valid, informed consent; and regulatory submissions and IRB processes.