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.
This program will entitle you:
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- Over 10 hours of powerful course content 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
- Full lifetime access
- 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
7 days money back guarantee
Accreditations
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
Professor 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, Professor 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, Professor Mitra has successfully led numerous high-profile clinical trials, securing over £10 million in grant funding and publishing more than 150 academic articles. 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, Professor 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
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.
Program Pricing
On Demand Learning
USD 490
- Lifetime access to high-quality self-paced eLearning content curated by industry experts
- 24x7 learner assistance and support
- Attain your Certified Clinical Research Project Manager (CCRP™) designation that you can use across your professional credentials
- Exhibit your professional acumen in developing and implementing clinical research projects, protocols, and procedures, while demonstrating expertise in project planning, budgeting, timelines, risk management, and team leadership.
- Over 10 hours of in-depth learning on clinical research project management, covering essential topics such as clinical trial design, regulatory compliance, project planning, budgeting, risk management, and team leadership, as well as best practices in data management, quality assurance, and stakeholder engagement.
- 5 powerful global case studies and best practices highlighting innovative research methodologies, effective protocol design, robust ethical frameworks, adaptive study designs, and strategic stakeholder engagement in clinical research management.
- Full lifetime access
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Corporate Training
Customized To Your Needs
- If you have more than 30 participants from your organizations, you can contact us to host a program customized to your training needs through a blended learning or physical classroom model
- By customizing your program, the faculty leader can tailor the content that is specific to your needs
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Prior to the commencement of the bespoke program, we will schedule conference calls to identify your training needs and map out the sessions most relevant to your organization
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
100% Money Back Guarantee
We value the trust of our customers immensely. But, if you feel that this Certified Clinical Research Project Manager (CCRP™) does not meet your expectations, we offer a 7-day money-back guarantee. Just send us a refund request via email within 7 days of purchase and we will refund 100% of your payment, no questions asked!
Certified Clinical Research Project Manager (CCRP™) Reviews and Testimonials
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Certified Clinical Research Project Manager (CCRP™)
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