Fully Accredited Program Certified Clinical Research Project Manager (CCRP™)

The clinical research industry has exploded in recent years, with global spending on clinical trials projected to reach $68.9 billion by 2026. However, managing these complex clinical trials remains incredibly challenging. Up to 85% of trials experience delays and each day of delay cost an average of $1.3 million of losses per day with delayed drug approvals and compromised data quality.

This certified program is designed to empower you with the advanced knowledge and skills needed to lead and execute clinical research projects with excellence. By integrating foundational principles with detailed case studies and best practices, you will gain a deep understanding of critical areas such as protocol development, regulatory compliance, study design, data management, quality oversight, budgeting, and and all other core project management functions. The program will also explore key topics including research history, protocol components, ethical approvals, adaptive study designs, patient recruitment and retention, risk management, and effective leadership in clinical research environments.

Throughout the program, you will learn how leading institutions successfully design and implement research protocols, navigate complex regulatory landscapes, and effectively manage every stage of a clinical study from inception to completion. You will develop the ability to craft robust research proposals, identify necessary skills and resources, plan and coordinate ethical submissions, and manage stakeholder expectations. This training will equip you to conduct comprehensive risk assessments, implement risk mitigation strategies, and adapt to emerging challenges while maintaining rigorous standards of Good Clinical Practice (GCP) and data integrity.

Additionally, the program will provide invaluable insights into managing patients and public involvement (PPI), enhancing patient recruitment and retention strategies, and fostering inclusive research practices. You will be trained to leverage digital tools, understand MedTech and digital research pathways, and optimize project management processes such as budgeting, contract negotiation, and team leadership.

Upon completing the program and passing the Chartered exam, you will be attaining the Certified Clinical Research Project Manager (CCRP™) designation that can be used in your professional credentials. This designation signifies your expertise in designing, executing, and managing impactful clinical research studies. In addition, this industry-recognized certification holds lifelong validity and is a testament to your leadership in the evolving landscape of clinical research.

4.6 (936 Professional Learners) 1

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This program will entitle you:

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  • Experience 3 days of instructor-led live program and gain comprehensive insights into clinical research project management, covering essential topics from robust protocol design, navigating complex regulatory pathways, and implementing adaptive study designs.
  • By the end of the program, you will earn the Certified Clinical Research Project Manager (CCRP™) designation, validating your proficiency in clinical research design, implementation, and management
  • Gain hands-on experience in leveraging advanced tools and methodologies for effective data management, patient recruitment, regulatory compliance, and project coordination, empowering data-driven decision-making and strategic planning
  • For inquiries, chat with our Program Advisers at advisor@charteredcertifications.com or call us at
    • Singapore and Asia Pacific: +65 6716 9980
    • Australia and New Zealand: +61 3 9909 7310
    • UK, Europe and Middle East: +44 (020) 335 57898
    • USA: +1 888 745 8875

Accreditations

4.8 

This Certified Clinical Research Project Manager (CCRP™) designation represents the highest standard of professional excellence in clinical research management. This credential validates comprehensive expertise across protocol development, regulatory compliance, risk management, team leadership, and stakeholder collaboration—establishing you as qualified experts in the efficient and ethical execution of clinical research initiatives. It is accredited by the Chartered Institute of Professional Certifications, which maintains the governing standards for all members. The CCRP™ charter is a trademarked charter available only to professionals who have completed and passed this program. The certification is governed and maintained by Chartered Institute of Professional Certifications with over 90,000 members around the world. It is also endorsed by prominent associations and organizations worldwide.

The content of this program has been fully certified and accredited by CPD as conforming to Continuing Professional Principles

What Can You Expect From This Certified Program

Effective clinical research project management has the potential to accelerate clinical trial completion by 15–20%, significantly reducing the time it takes for therapeutic innovations to reach patients. However, clinical project managers face considerable challenges, including stringent cost management, navigating complex regulatory frameworks, and ensuring seamless coordination among diverse stakeholders.

This certified program will equip clinical leaders with the advanced skills and knowledge required to overcome these challenges effectively, guiding you through the entire research lifecycle from design and implementation to monitoring and closeout. You will explore essential frameworks including protocol development, ethical approvals, regulatory compliance, and risk mitigation strategies, as well as innovative approaches like adaptive and decentralized trial designs. The program emphasizes practical application, focusing on resource allocation, stakeholder engagement, patient recruitment, data integrity, and team leadership, helping you understand the interplay between planning, execution, and compliance in clinical research.

Beyond understanding frameworks, this program will teach you how to create and implement effective project management strategies tailored to the clinical research context. You will gain skills to conduct thorough risk assessments, develop robust protocols, manage budgets and contracts, and ensure adherence to Good Clinical Practice (GCP). Moreover, you will delve into critical topics such as patient and public involvement, regulatory pathways for MedTech and digital research, and strategies for overcoming common challenges like delays and budget overruns. By completing this program, you will not only enhance your knowledge of clinical research management but also be able to integrate best practices into your projects, ensuring efficiency, regulatory compliance, and innovation.

Upon completing the program and passing the Chartered exam, you will attain the Certified Clinical Research Project Manager (CCRP™) designation. This credential will signify your expertise in designing rigorous study protocols, expertly navigating complex regulatory frameworks, implementing proactive risk mitigation strategies and leading multidisciplinary teams to execute compliant, efficient, and high-impact research initiatives.

Key Skills You Will Gain

  • Clinical Research Protocol Design
  • Regulatory Compliance Navigation
  • Risk Management and Mitigation
  • Stakeholder Engagement and Communication
  • MedTech Integration & Innovation Interventional Study Design
  • Adverse Event Reporting
  • Research Data Governance
  • Biostatistics and Statistical Analysis
  • Ethics and Informed Consent
  • Budget Development & Financial Oversight Regulatory Inspections and Audits
  • Site Selection and Management
  • Data Management and Analysis
  • Patient Recruitment & Retention Strategies
  • Alternative Research Design Implementation Good Clinical Practice (GCP) Standards
  • Clinical Trial Monitoring
  • Quality Assurance Protocols Ethics Submissions and Approvals
  • Non-Interventional Research Studies
  • Device Related Research Conduct
  • Clinical Research Team Management
  • Clinical Trial Close-Out and Reporting
  • Clinical Research Documentation & Record-Keeping
  • Patient and Public Involvement (PPI)

Your Faculty Director

Dr Sandip Mitra
Dr Sandip Mitra
Award-Winning Clinical Research Expert

Dr. Sandip Mitra is a distinguished expert with over 20 years of experience in clinical research and nephrology. He is a leading authority committed to advancing the fields of clinical trials and dialysis medicine through innovative research, education, and compassionate patient care. Throughout his career, Dr. Mitra has held several prominent leadership roles, including Consultant Nephrologist, Clinical Lead, and Principal Investigator, across academia, healthcare, and industry.

As a renowned clinical researcher, Dr. Mitra has successfully led numerous high-profile clinical trials, securing £1.9 million in grants and publishing 39 papers. His expertise has also empowered countless researchers and healthcare professionals in clinical research project management, dialysis medicine, and blood purification techniques.

Recognized for his exceptional contributions to clinical research, Dr. Mitra has received 12 national awards, including the prestigious HSJ Top 50 UK Innovator in Healthcare award. He is a highly regarded opinion leader, advisor, and reviewer, with academic affiliations and memberships in prestigious organizations, further cementing his status as a trusted authority in his field.

Certified Clinical Research Project Manager (CCRP™) Program Agenda

Module 1 - Introduction to Clinical Research
Module 2 - Clinical Research Protocols
Module 3 - Clinical Research Process and Pathways
Module 4 - Alternative Research Designs
Module 5 - MedTech and Digital Research Projects
Module 6 - Patient Participation & Recruitment
Module 7 - Clinical Research Project Management - Part 1
Module 8 - Clinical Research Project Management - Part 2
Module 9 - Good Practice & Data Management
Module 10 - Leadership and Excellence in Clinical Research
Examination

Chartered Exam

At the end of the program, there will be a Chartered exam comprised of 50 multiple choice questions. Upon passing the exam, you will be accredited with Certified Clinical Research Project Manager (CCRP™) designation.

  • 98% of students who have taken this exam have passed the exam successfully. Almost all professionals who have taken our courses have passed this exam and attain their Certified Clinical Research Project Manager (CCRP™) designation
  • The exam has 50 multiple choice questions and you need to answer 25 out of 50 questions correctly to pass the exam
  • You can re-take the exam online as many times as you want, with no additional charges for retaking of exams
  • The program cost already includes the exam fees, so there are no additional charges for taking the exam

If you have challenges passing the exam, you can secure assistance from our team and faculty leader to help you pass the exam.

Certified Clinical Research Project Manager (CCRP™) Designation

Upon completion of the program and successfully passing the Chartered exam, you will be awarded the prestigious Certified Clinical Research Project Manager (CCRP™) designation, which can be showcased in your resume, CV, and other professional credentials. Developed by the esteemed Chartered Institute of Professional Certifications, a leading authority in professional certifications, this industry-recognized, trademarked charter positions you as an expert in managing clinical research projects. It demonstrates your extensive knowledge and expertise in planning, executing, and delivering complex clinical research, while highlighting your proficiency in applying project management principles, methodologies, and best practices to drive success, ensure regulatory compliance, and foster advancements in medical innovation.

The program's content has been independently accredited and certified by the Continuing Professional Development (CPD) organization, guaranteeing adherence to rigorous standards of professional development.

Pricing & Registration

Please select one of the locations:

United Kingdom

Dates: 11 - 13 Jun 2025

Venue: Online Executive Program (via Zoom)

Time: 9:00am - 4:30pm British Summer Time (BST)


Early Bird Packages Regular Pricing
By 08 Apr 2025 By 20 May 2025 After 20 May 2025
UK Delegates GBP 1,495 GBP 1,695 GBP 1,795

Group Discount: 2nd participant get 10%, or register 3 participants and 4th participant get a complimentary seat (1 discount scheme applies)

Register Now

Download Brochure

You can download our program brochure below. If you have any inquiries on this program, please contact our Program Advisor at advisor@charteredcertifications.com or call us at:

  • Singapore and Asia Pacific: +65 6716 9980
  • Australia and New Zealand: +61 3 9909 7310
  • UK, Europe and Middle East: +44 (020) 335 57898
  • USA: +1 888 745 8875

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On Demand Learning

If you are unable to make it to this program due to the dates, you can also enroll into our program through our on-demand learning. Click on the link below to go to our on demand learning to discover how you can enroll into the program and earn your Charter or certificate through our on demand learning platform

Go to Our On Demand Learning Here

Convincing Your Boss To Attend This Program

Securing approval from your boss to attend this program can be difficult if you don’t know what to say. So we’ve prepared a template for you! All you need to do is to download this template, copy and paste in email and send it to your boss!

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Certified Clinical Research Project Manager (CCRP™)

4.6 (936 ratings)