VIARES ACADEMY Courses

ALL for the price of 2

VIARES ACADEMY ALL-In-One

ALL courses for the price of 2! Transform your clinical research career with our comprehensive training bundle! By enrolling in all courses, you’ll gain expertise across trial documentation, monitoring trials, project and site management, regulatory compliance, oncology research, remote monitoring and all you need for your clinical research career.

TOP COURSE

Clinical Research Associate

Step into the role of a Clinical Research Associate! This course covers clinical trial management, regulatory compliance, and data quality. Master the skills to monitor trial sites, ensure patient safety, and support groundbreaking research—your career in clinical research starts here.

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Navigating ICH GCP E6(R3)

Navigate ICH-GCP E6(R3) standards with confidence! This course provides comprehensive training on ethical guidelines, regulatory compliance, and trial management. Gain the expertise needed to ensure high standards in clinical trials worldwide—start enhancing your clinical research knowledge today!

Clinical Research Project Manager

Grow your career in Clinical Project Management with our Academy! Build your new skills around Project Management , Stakeholder Management, Risk Management, Budgeting and many other job-relevant skills, to step our of your current role and become a Clinical Project Manager.

Clinical Study Coordinator I

Launch your career as a Clinical Study Coordinator! This course provides essential skills in study design, site management, and regulatory compliance, preparing you for a pivotal role in clinical trials. Gain practical knowledge to support groundbreaking medical research—your journey starts here.

Study Start Up Specialist

Become a Study Start-Up Specialist and master the processes that bring clinical trials to life. Learn key regulatory requirements, submission strategies, and project initiation skills to ensure compliance and efficient trial launches. Start building your expertise in clinical research today!

Trial Master File Specialist

Jumpstart your career in clinical research! Gain essential TMF skills to manage trial documentation, ensure compliance, and meet regulatory standards. Become the specialist top organizations need—enroll now and elevate your expertise in clinical trial management.

Clinical Operations Specialist

Drive clinical trial success as a Clinical Operations Specialist! This course gives you expertise in trial design, regulatory compliance, and site management to ensure seamless operations. Build a career in clinical research with skills that global organizations value—start now!

Clinical Research Project Specialist

Accelerate your career as a Clinical Research Project Specialist! This course equips you with skills in project design, compliance, and stakeholder communication. Learn to manage clinical trials effectively, ensuring successful project outcomes. Start making an impact in clinical research now!

Clinical Trials Assistant

Start your journey as a Clinical Trials Assistant! This course gives you foundational knowledge in clinical research, trial documentation, and data management. Learn essential skills to support clinical trials efficiently, making a real impact in the field of medical research—enroll now and start building your expertise!

Remote & Centralized Monitoring

Master remote and centralized monitoring for clinical trials! This course equips you with regulatory knowledge, risk-based monitoring skills, and daily workflows for remote oversight. Start shaping your expertise in modern monitoring methods to excel in clinical research—enroll today!

Clinical Study Coordinator II

Advance your skills as a Clinical Study Coordinator! This course covers ALCOA-CCEa principles, patient consent management, and precise data handling. Gain critical expertise in eligibility assessment, adverse event management, and documentation accuracy—step up in clinical research now!

Clinical Study Coordinator III

Advance as a Clinical Study Coordinator! Gain expertise in IRB management, regulatory compliance, and precise trial documentation. Build specialized skills in FDA forms, protocol deviations, and investigational product handling—excel in complex clinical research responsibilities today

The Oncology CRA

Specialize as an Oncology CRA! This course provides key skills in oncology trial monitoring, patient safety, and compliance with industry standards. Gain expertise in managing complex oncology trials and become a valuable asset in clinical research—start advancing your career in oncology today!