Practical, Self-Paced Training for Every Step of Your Clinical Research Career
Whether you're breaking into clinical research, preparing for promotion, or moving from site to sponsor, our expert-designed courses give you the tools, knowledge, and clarity to grow with confidence. Click any course to go get instant access. No fluff. No wait. Just real training.
Core Skills
Core Skills for Clinical Research Professionals

GCP Essentials for Job Seekers
Understand the foundational ethics and compliance principles behind every trial. Includes job-ready talking points for interviews.

Clinical Trial Phases & Design Explained
Master the 4 phases of trials and understand how study design decisions impact data, safety, and endpoints.

Stakeholders in Clinical Trials: Site, CRO, Sponsor
Learn how research teams interact, who owns which responsibilities, and how to communicate across functions.
Advanced Training
Advanced Clinical Operations Training

eTMF Essentials for Site and Sponsor Teams
Learn what belongs in the Trial Master File, how documents are categorized, and how to maintain compliance.

Clinical Trial Documentation Mastery
Everything you need to know about ICFs, Source Documentation, Protocol Deviations, Monitoring Reports, and QC practices.

CTMS, EDC & Clinical Data Systems Overview
Get up to speed on the key technology platforms used in trial management and data entry—includes real case flow examples.
Compliance & Guidelines
Regulatory Compliance & Global Guidelines

U.S. Regulatory Compliance (FDA-Focused)
Deep dive into 21 CFR Part 11, FDA inspection expectations, IND/NDA basics, and sponsor obligations under U.S. law.

European Compliance & EMA Guidelines
Understand EMA clinical trial application (CTA) process, EudraCT, EU CTR, GDPR for trials, and Sponsor/Investigator duties under EMA regulations.

ICH E3 – Clinical Study Report Guidance Explained
Learn how to structure, write, and QC a CSR using ICH E3 with examples and interpretation tips.
Finance, Budgeting & Contracts
Finance, Budgeting & Contracts

Clinical Trial Budgeting & Site Contract Fundamentals
Learn how budgets are built, how to negotiate site budgets, and how to spot red flags in contract clauses.

Sponsor-CRO Agreements & Payment Schedules
Ideal for CTMs and PMs. Walk through negotiation strategy, budget schedules, and CRO oversight expectations.
Specific Prep Courses
Role-Specific Prep Courses

The CRA Role: Daily Tasks, KPIs & Tools
Get inside the mind of a CRA. Includes visit timelines, trip report walkthroughs, and performance metrics.

CRA vs. CTA vs. CRC: Role Comparison Masterclass
Perfect for job seekers who want to understand which role fits their skills and growth plan.
Career & Interview
Career & Interview Prep (DIY Toolkits)

DIY Resume Revamp Kit
ATS-friendly templates, value-based resume writing tutorials, keyword maps, and before/after examples.

Interview Mastery for Clinical Research Roles
Includes 40+ clinical operations questions, STAR story builder, mock interview scripts, and role-specific answers.

LinkedIn Visibility Plan (7-Day Challenge)
Step-by-step guide to increase visibility, optimize your profile, and connect with recruiters.
Career Bundles
Career Bundles (High-Value Combos)

Clinical Research Career Starter Bundle
Includes: GCP Essentials + Trial Phases + Stakeholders + Resume Toolkit

Site to CRO/CRA Transition Pack
Includes: CRA Role Course + eTMF Essentials + Monitoring Report Examples + Interview Scripts.

Clinical Research Compliance Pack (Global)
Includes: FDA Compliance + EMA Guidelines + ICH E3
Why Us
Why Choose YANA Courses?
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Built by real clinical research leaders (not generic educators)
Role-specific, practical, and jargon-free
Self-paced and designed for action
Instant lifetime access
Stackable with coaching programs
“These are the courses I wish I had when I started in research—and the ones I now use to train my own teams.”
— Coach Rudy

FAQs
Frequently Asked Questions
Are these for beginners or experienced professionals?
Will I get a certificate?
Can I bundle courses or apply them toward coaching?
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