Name: Lisa-Pierre
Item: CCRPS Clinical Research Training
Rating: 5
Author: admin

Leading Research Assistant Training Program

Start or advance as a Research Assistant with our leading, triple‑accredited, 100% online, self‑paced research assistant certification and training program—114 advanced topics for 2025, live webinars, mentorship, 8 years of alumni success, earn your certificate and LinkedIn badge, and boost your salary potential to $45K–$65K+; call 24/7 at +1 (239) 329-9837 with a 14‑day refund policy.

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Start Your Career As An Advanced Clinical Research Assistant

Gain research experience and get paid while you learn with our industry-recognized program. Designed for high school graduates and premeds, this training opens doors to high-demand roles with earning potential up to $60k+. 100% Money-back Guarantee with 14 Day Refund Policy. Payment Plans Available.

$299.00

112 In-Depth Advanced Research Assistant Training Modules ($1000 Value). 50 Page ACTAC Study Guide + Certification Exam Backed by ACCRE. Lifetime Access to Unmatched Curriculum.

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$5,000.00 / year

Organizational ACTAC Licensing

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$1,299.00

w/ Mentorship & Mastery Prep

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Clinical Research Assistant Training

Advanced Clinical Research Assistant Certification

1. CME Handout
2. Live Review Webinar - See discussion for next meeting date
1. The Primary Purpose of Clinical Research in Medicine
2. How Historical Events Shaped Modern Research Ethics
3. The Four Phases of Clinical Trials: Focus and Application
4. The Role of Institutional Review Boards (IRBs) in Clinical Research
5. Good Clinical Practice (GCP): Definition and Importance in Clinical Trials
6. Core Responsibilities of an Investigator in a Clinical Trial
7. How Research Assistants Support Clinical Trials at Various Phases
8. Importance of Patient-Centered Research in Modern Clinical Trials
9. Ethical Principles in the Declaration of Helsinki
10. Essential Elements for Developing a Clinical Trial Protocol
1. An Introduction to Clinical Research
2. An Overview of ICH GCP
3. Code of Federal Regulations
4. CFR 21 Part 11
1. Sponsor/CRO Responsibilities
2. 13 Principles, IRB, & Investigator Roles
1. Informed Consent
2. Safety of Human Subjects in Clinical Research
1. Reporting Responsibilities of the Investigators
2. Adverse Events
1. Ethics of Research Involving Children
2. Ethics of Research Involving Mentally Incapacitated
3. Ethics of Research Involving Pregnant Women and Fetuses
4. Ethics of Research Involving Prisoners
1. Trial Management – Data Handling and Record Retention
2. a) Common Terminology Used In Clinical Research
3. b) Commonly Used Abbreviations and Terms in Clinical Research
1. Advanced Designs of Clinical Trials
2. Advanced Review of Phases of Clinical Trials (Preclinical & Phase 0-4)
1. Patient Recruitment in Clinical Trials
2. Patient Engagement and Retention in Clinical Trials
3. Patient Adherence and Compliance in Clinical Trials
1. Scientific Misconduct and Fraud
2. Detecting Falsification
1. Key Features of Randomized Controlled Trials (RCTs)
2. How Adaptive Clinical Trials Differ from Traditional Trial Designs
3. Benefits and Challenges of Decentralized Clinical Trials
4. Importance of Feasibility Analysis in Clinical Trial Planning
5. Differences Between Clinical Research and Laboratory Research
6. Strategies for Recruiting Participants for Rare Disease Trials
7. Unique Considerations in Designing Trials for Vulnerable Populations
8. How Resource Limitations Affect Trial Site Planning
9. Translational Research: Bridging Basic Science to Clinical Trials
10. Tailoring Recruitment Strategies for Difficult-to-Enroll Populations
1. Key Principles of the Belmont Report and Their Modern Relevance
2. Global Research Regulation: FDA vs. EMA
3. HIPAA Privacy Standards in Clinical Research
4. GDPR's Impact on Multinational Clinical Trials Involving EU Participants
5. Ethical Challenges in Pediatric Research
6. Preventing Scientific Misconduct in Clinical Trials
7. The Process for Reporting Serious Adverse Events (SAEs) Ethically
8. Compassionate Use Trials and Ethical Considerations
9. Regulatory Oversight for Gene Therapy Clinical Trials
10. Ethical Review and Monitoring of Expanded Access Programs
1. Strategies to Improve Patient Recruitment in Longitudinal Studies
2. Importance of Building Trust in Trial Recruitment
3. Benefits of Cultural Competence in Recruitment
4. Unique Challenges in Recruiting Pediatric Patients for Clinical Trials
5. Enhancing Recruitment with Technology in Rural and Global Scenarios
6. Role of Patient Advocacy Groups in Promoting Trial Participation
7. Strategies to Improve Retention in Multi-Year Clinical Trials
8. Minimizing Disparities in Clinical Trial Access
9. Key Principles of Culturally Sensitive Communication
10. Importance of Diversity in Global Clinical Trials and Strategies to Achieve It
1. Features Differentiating EDC Platforms from Traditional Data Entry
2. Ensuring Data Integrity Through Query Resolution
3. Purpose of a Clinical Trial Management System (CTMS)
4. Techniques to Ensure Accurate Anonymization of Participant Data
5. Preparing Sites for Audits: A Guide for Research Assistants
6. Importance of Data Validation in Clinical Trials
7. Role of Case Report Forms (CRFs) in Documentation Management
8. Improving Clinical Research Data Analysis with Statistical Tools
9. Best Practices for Ensuring Consistency Across Multi-Site Data Collection
10. Ethical Considerations for Managing Patient-Related Trial Data
1. Key Responsibilities of CRAs During Monitoring Visits
2. On-Site vs. Remote Monitoring in Clinical Trials
3. How Risk-Based Monitoring Improves Clinical Trial Efficiency
4. Challenges in Source Data Verification (SDV)
5. Role of a Sponsor in Data Safety Reviews
6. Managing Disparities in Multi-Country Trials
7. Indicators of Potential Protocol Deviations
8. Role of DSMBs in Clinical Trials
9. Preparing for Regulatory Inspections
10. Importance of Standardization in Multi-Site Trials
1. Delegating Responsibilities in Clinical Research Teams
2. Enhancing Team Collaboration Through Effective Communication
3. Ensuring Accountability in Research Teams
4. Supporting Trial Sponsors During Execution
5. Importance of Conflict Resolution in Multi-Disciplinary Research Teams
6. Role of Coordinators in Bridging Sites and Sponsors
7. Leadership Strategies for Experienced Research Assistants
8. Importance of Training and Mentorship in Research Teams
1. Unique Challenges in Gene Therapy Trial Design
2. Importance of Rare Disease Research in Advancing Medicine
3. Common Endpoints in Cardiology Clinical Trials
4. Impact of Pharmacogenomics on Personalized Medicine
5. Safety Considerations in Regenerative Medicine Trials
6. Role of Biomarkers in Neurology Research
7. Ethical Implications of Trials in Palliative and End-of-Life Care
8. Benefits of Combining Therapies in Hybrid Trials
9. Enhancing Asthma and COPD Trials with Wearable Medical Devices
1. Certifications for Entry-Level Research Assistants
2. Enhancing Career Development in Clinical Research Through Networking
3. Importance of Time Management Skills for Research Assistants
4. Valued Leadership Traits in Research Operations
5. Mentorship in Sustainable Career Pathways
6. Lateral Growth Opportunities for Research Assistants
7. Trends Redefining Roles in Technology-Enhanced Studies
8. Building a Competitive CV in Clinical Research
9. Preparing for Transition to CRA or Study Coordinator Roles
10. Lifelong Learning and Career Longevity in Clinical Trials
1. Research Assistant Competency Exam (25 Questions)

$299.00
114 lessons
3 Weeks
HS/GED Required. Perfect for Premeds or Transitioning To Clinical Trials.
Salary $25k–$70k

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Why choose our research assistant program?

Turn Your Love for Science into a Rewarding Career

Passionate about science? Take the first step in healthcare with our Clinical Research Assistant Training. Gain hands-on research experience and earn $25k–$70k+ annually—with even greater potential as you advance.
Learn Skills that Fast-Track Promotions

Want to climb the ladder faster? Master essential skills like trial management, patient safety, and ethical compliance that prepare you to step into coordinator and monitoring roles.
Jump into Clinical Research Coordinator (CRC) Roles

Get ahead of the game with specific training designed to prepare you to easily transition to CRC roles. Lead clinical trials, manage teams, and take charge of breakthrough healthcare studies early in your career.

CCRPS Reviews

Research Assistant Certification Reviews

EXCELLENT!

Eliana Vasquez Barthon

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Cert

ANKIT Bais

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Good Course with great self learning mechanism

Yudha Ferriansyah

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Research Assistant

ADOLFO Enrique GONZALEZ ALEMAN

Excelente course! Some lectures are a bit quick and one has to hear them again

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Fundamentals of Clinical Trials

Michelle Porter

The course was very informative and relevant to the job that I currently do.

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Excellent presentation, truly enjoyed the course!

Anupama Ubriani

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Excellent

Wendy Donkor

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Good Course with great self learning mechanism

Yudha Ferriansyah

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CTA

Grace Badejo

Material was explanatory.

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Fundamentals of clinical research

Paul Macaire OSSOU-NGUIET

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Research Assistant Grads Hired As:

Clinical Research Assistant, Research Assistant, Research Study Assistant, Trial Assistant, Clinical Trial Assistant, Assistant Clinical Research Coordinator, Assistant Clinical Trials Administrator, Clinical Project Assistant, Clinical Research Coordinator, Clinical Researcher Professional, Clinical Study Coordinator, Clinical Trial Coordinator, Patient Recruitment Coordinator, Regulatory Affairs Assistant (2024 CCRPS Graduate LinkedIn Survey).

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Elevate Your Career with CCRPS Advanced Clinical Research Assistant Training

Become a Certified Clinical Research Assistant with CCRPS - Gain the Credentials That Stand Out With Our 26,000 Member Clinical Research Community

Industry-Leading Clinical Research Assistant Training

Unlock your potential in clinical trials with CCRPS. Our 150-hour instructor-led program offers everything you need to excel as a certified research assistant. Whether you're just starting or looking to enhance your skills, this clinical research assistant course empowers you to step confidently into clinical research.

Why Enroll?

Comprehensive Curriculum
Gain expertise in trial management, compliance, and data analysis through our in-depth research assistant training program. Learn skills that employers in clinical research demand.
Globally Recognized Certification
Upon completing the clinical research assistant training course, earn a clinical research assistant certificate valued worldwide. Boost your credibility and job prospects.
Real-World Applications
From ethical research to patient recruitment, this research assistant program bridges the gap between theory and practice. It’s perfect for those pursuing medical research assistant training or wanting to refine their skills using a research assistant training manual.

Program Highlights

Master global standards like ICH-GCP and compliance strategies in clinical trials.
Develop patient safety protocols using employee assistance program research methods.
Handle documentation, protocol adherence, and advanced trial coordination.

FAQ

1. Who Should Take This Course?

This clinical research assistant certification is perfect for beginners, students, and experienced professionals seeking to specialize in clinical trials.

2. What Can I Expect to Learn?

Gain hands-on skills in trial logistics, data compliance, and using advanced tools for ethical research, guided by an accessible research assistant training manual.

3. Is the Certification Recognized?

Yes, this research assistant certification is globally respected, equipping you for roles in top CROs, pharmaceutical companies, and clinical trial organizations.

4. How Long Does It Take?

This research assistant course is self-paced, typically completed in 3 weeks with lifetime access for updates.

5. What Roles Can I Pursue?

Graduates are equipped for roles like Clinical Trial Assistant, Data Coordinator, and Certified Research Assistant.

Start your career transformation with CCRPS, the leader in clinical research assistant programs.

👉 Enroll Now in the Clinical Research Assistant Training Course and take the first step in building a rewarding career!

$299.00

$5,000.00 / year

$1,299.00

Introduction

CH 1. Wk 1 Foundations of Clinical Research

CH 2. Wk 1 Fundamentals of Clinical Research

CH 3. Wk 1 Clinical Trial Roles and Responsibilities

CH 4. Wk 1 Informed Consent & Patient Safety

CH 5. Wk 1 Adverse Event Reporting & Responsibilities

CH 6. Wk 2 Ethical Research in Vulnerable Populations

CH 7. Wk 2 Trial Management, Data Handling, and Record Retention

CH 8. Wk 2 Clinical Trials - Advanced Review

CH 9. Wk 2 Subject Recruitment, Retention, and Compliance

CH 10. Wk 2 Misconduct and Fraud

CH 11/12. Wk 3 Clinical Trial Design and Planning

CH 13. Wk 3 Ethical and Regulatory Landscape

CH 14. Wk 3 Patient Recruitment, Retention, and Diversity

CH 15. Wk 3 Data Management and Documentation

CH 16. Wk 4 Monitoring, Oversight, and Quality Assurance

CH 17. Wk 4 Monitoring, Oversight, and Quality Assurance (Continued)

CH 18. Wk 4 Advanced Therapeutic Areas and Clinical Niches

CH 19. Wk 4 Career Development for Clinical Research Assistants

CH 20. Wk 4 Clinical Trial Assistant Certification Exam

Turn Your Love for Science into a Rewarding Career

Learn Skills that Fast-Track Promotions

Jump into Clinical Research Coordinator (CRC) Roles

Industry-Leading Clinical Research Assistant Training

Why Enroll?

Program Highlights

FAQ

1. Who Should Take This Course?

2. What Can I Expect to Learn?

3. Is the Certification Recognized?

4. How Long Does It Take?

5. What Roles Can I Pursue?