Female clinical research coordinator in modern medical office reviewing trial documentation on a tablet with clinical equipment in the background
Female clinical research coordinator in modern medical office reviewing trial documentation on a tablet with clinical equipment in the background
Medimar Academy

How to Coordinate Clinical Trials

Master practical site coordination from feasibility and protocol startup through trial closeout. Gain real-world operational workflows for running compliant, high-performing clinical studies.

Program Overview

Built for Practical Clinical Impact

A comprehensive online training program built to prepare coordinators for real site operations and regulatory compliance.

Target Audience
Skill Mastery
Delivery Format

Who This Course Is For

Learning Outcomes

Course Materials & Format

Current and aspiring Clinical Research Coordinators (CRCs), site nurses, study assistants, and life science graduates entering site management.

Master study startup, patient recruitment, protocol compliance, EDC data entries, IP accountability, audit readiness, and AI-driven site workflows.

Includes 10 on-demand video modules, interactive knowledge quizzes, downloadable site SOP templates, and automated progress tracking.

— 10-Module Syllabus

Complete Course Curriculum

Explore every phase of trial coordination through ten structured modules designed by experienced clinical operations professionals.

Modules 01 - 05

Modules 06 - 10

Module 1: Site Systems & Administration Foundational site infrastructure, regulatory frameworks, and team structure.

Module 6: Safety & Investigational Product Adverse event (AE/SAE) reporting, IP accountability, and temperature logs.

Module 2: Feasibility & Protocol Startup Evaluating study protocols, budget feasibility, and IRB/EC submission steps.

Module 7: Essential Records, Deviations & CAPA Managing Trial Master File (TMF) docs, protocol deviations, and corrective plans.

Module 3: Delegation & Team Training Maintaining Delegation of Authority (DOA) logs and staff training records.

Module 8: Decentralized Trials & Vendors Managing ePRO, wearable devices, home health nursing, and third-party vendors.

Module 4: Recruitment & Informed Consent Patient engagement strategies and legal/ethical informed consent execution.

Module 9: Responsible AI in Site Coordination Leveraging ethical AI tools to streamline participant scheduling and tracking.

Module 5: Visits, Source Data, EDC & Queries Conducting subject visits, source documentation, EDC entry, and query resolution.

Module 10: Closeout, Inspection & Integrated Case Study termination, regulatory audit readiness, and an integrated real-world case.

• Enrollment Details

$195 USD

Promotional Price (Regular $249 USD)

Advance Your Clinical Research Career Today

Includes full access to 10 video modules, downloadable resources, and completion certificate.

Get immediate lifetime access to all 10 video modules, practical site templates, module quizzes, and automated progress tracking upon enrollment.

Training and support in Clinical Research

mgarcia@medimarsolutions

305-6103464

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