CCRPS

CPD Standards Office Provider Number: 50670

Send an enquiry

Send an enquiry to this training provider

Name(Required)

Surname(Required)

Phone

Email(Required)

Message(Required)

Spam Check: How Much is 7 multiplied by 6?(Required)

Please enter a number from 41 to 43.

This field is hidden when viewing the form

Email of contact

This field is hidden when viewing the form

CPD Standards Office Provider ID

This field is hidden when viewing the form

Accredited Activities

<ul>
 	<li>Clinical Research Associate Training</li>
</ul>
290 Hours - 4 Weeks Agenda
Develop advanced skills for monitoring clinical trial processes and maintaining data integrity across multiple trial specialities and designs.
Understand compliance with FDA and ICH-GCP standards for trial oversight.
Learn site management, risk assessment, and communication with stakeholders.
Online course
Professionals aiming to start or advance their careers as Clinical Research Associates (CRAs). This includes individuals with some clinical research experience or those transitioning from related fields like healthcare or science. The program is designed for those seeking advanced monitoring skills across various trial types and specialities.
<a href="https://app.ccrps.org/courses/cra">https://app.ccrps.org/courses/cra</a>
<ul>
 	<li>Clinical Research Coordinator Training</li>
</ul>
110 Hours - 3 Weeks Agenda
Master participant recruitment, consent processes, and trial documentation.
Understand regulations, ethical considerations, and trial logistics.
Enhance proficiency in data collection and protocol adherence across specialities.
Online course
Aspiring CRCs such as those with a minimum of 2 2-year degree (RN or LPN okay) and some patient experience. As well as Clinical Research Coordinators (CRCs) with experience to bridge knowledge gaps, tailored for professionals looking to enhance their expertise in managing clinical trials, including project management, compliance, and data management.
<a href="https://app.ccrps.org/courses/Clinical-Research-Coordinator">https://app.ccrps.org/courses/Clinical-Research-Coordinator</a>
<ul>
 	<li>Pharmacovigilance and Regulatory Affairs Training</li>
</ul>
170 Hours - 4 Weeks Agenda
Gain expertise in monitoring and reporting drug safety and adverse reactions.
Learn risk assessment and global compliance standards (FDA, EMA).
Establish communication skills to relay safety data to regulatory bodies.
Online course
Professionals with prior experience in clinical research or healthcare, such as physicians, pharmacists, or regulatory specialists. This program is ideal for those focusing on pharmacovigilance, regulatory compliance, and safety monitoring in multinational clinical trials.
<a href="https://app.ccrps.org/courses/pharmacovigilance-certification">https://app.ccrps.org/courses/pharmacovigilance-certification</a>
<ul>
 	<li>Clinical Research Project Manager Training</li>
</ul>
290 Hours - 4 Weeks Agenda
Acquire leadership for managing clinical trials from initiation to closure.
Understand resource allocation, timeline adherence, and team coordination.
Learn risk mitigation strategies and problem-solving skills.
Online course
Professionals with prior experience in clinical research or project management, such as Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), or those transitioning into leadership roles. This program is ideal for individuals aiming to become Clinical Trial Managers, Research Project Managers, or Clinical Research Leaders.
<a href="https://app.ccrps.org/courses/Advanced-Clinical-Research-Project-Manager-Certification">https://app.ccrps.org/courses/Advanced-Clinical-Research-Project-Manager-Certification</a>
<ul>
 	<li>Good Clinical Practice Certification and Training 2025</li>
</ul>
70 Hours - 1 Week Agenda
Master global guidelines and ethical standards for clinical trials.
Develop detailed knowledge of sponsor and investigator obligations.
Learn proper documentation and reporting practices for trial data, including updates with E6 (R3) for 2025.
Online course
Designed for all professionals desiring to master good clinical practice guidelines to improve ethical and compliant clinical research. This includes all roles in clinical research as well as increased mastery for experienced Clinical Quality Assurance Professionals, Clinical Research Associates, Project Managers, Investigators, Study Coordinators, and Regulatory Affairs Professionals. It is required to retake every two years.
<a href="https://app.ccrps.org/courses/ich-gcp">https://app.ccrps.org/courses/ich-gcp</a>
<ul>
 	<li>Leading Research Assistant Training Program</li>
</ul>
114 Hours - 3 Weeks Agenda
Understand trial design basics and sample management tasks.
Learn regulatory documentation techniques and operational support skills.
Develop strong problem-solving capabilities within trial settings.
Online course
Entry-level professionals or those transitioning into clinical research roles. This program is suitable for individuals aiming to build foundational skills in trial design, protocol development, and data management.
<a href="https://app.ccrps.org/courses/Clinical-Trials-Assistant-Training">https://app.ccrps.org/courses/Clinical-Trials-Assistant-Training</a>
<ul>
 	<li>Medical Science Liaison - Medical Monitor Certification</li>
</ul>
250 Hours - 4 Weeks Agenda
Gain skills in reviewing trial protocols and assessing participant safety across multiple trial specialities and designs.
Learn adverse event management and medical oversight procedures.
Enhance communication with stakeholders to ensure trial efficacy and leadership.
Online course
Medical professionals such as MDs, IMGs, PharmDs, PhDs, and NPs are aiming to transition into roles like Medical Science Liaison (MSL) or Medical Monitor. This program is ideal for those seeking advanced skills in clinical trial oversight, regulatory compliance, and strategic medical communication.
<a href="https://app.ccrps.org/courses/medial-monitor-certification">https://app.ccrps.org/courses/medial-monitor-certification</a>
<ul>
 	<li>Principal Investigator Certification</li>
</ul>
179 Hours - 4 Weeks Agenda
Build expertise in leading clinical trials and overseeing participant safety across multiple trial specialities.
Learn protocol design, budget management, and compliance adherence.
Develop leadership and communication for collaboration with sponsors.
Online course
Physicians and healthcare professionals with an active medical license or prior experience as Sub-Investigators. This program is tailored for those aiming to lead clinical trials as Principal Investigators, focusing on trial design, sponsor collaboration, and regulatory compliance.
<a href="https://app.ccrps.org/courses/Advanced-Principal-Investigator-Physician-Certification">https://app.ccrps.org/courses/Advanced-Principal-Investigator-Physician-Certification</a>

This field is hidden when viewing the form

Who should attend

Professionals aiming to start or advance their careers as Clinical Research Associates (CRAs). This includes individuals with some clinical research experience or those transitioning from related fields like healthcare or science. The program is designed for those seeking advanced monitoring skills across various trial types and specialities.

CCRPS Advanced Clinical Research Associate Training
<ul>
 	<li>Aspiring CRCs such as those with a minimum of 2 2-year degree (RN or LPN okay) and some patient experience. As well as Clinical Research Coordinators (CRCs) with experience to bridge knowledge gaps, tailored for professionals looking to enhance their expertise in managing clinical trials, including project management, compliance, and data management.</li>
</ul>
CCRPS Advanced Clinical Research Coordinator Training
<ul>
 	<li>Professionals with prior experience in clinical research or healthcare, such as physicians, pharmacists, or regulatory specialists. This program is ideal for those focusing on pharmacovigilance, regulatory compliance, and safety monitoring in multinational clinical trials.</li>
</ul>
CCRPS Advanced Pharmacovigilance and Regulatory Affairs Training
<ul>
 	<li>Professionals with prior experience in clinical research or project management, such as Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), or those transitioning into leadership roles. This program is ideal for individuals aiming to become Clinical Trial Managers, Research Project Managers, or Clinical Research Leaders.</li>
</ul>
CCRPS Advanced Clinical Research Project Manager Training
<ul>
 	<li>Designed for all professionals desiring to master good clinical practice guidelines to improve ethical and compliant clinical research. This includes all roles in clinical research as well as increased mastery for experienced Clinical Quality Assurance Professionals, Clinical Research Associates, Project Managers, Investigators, Study Coordinators, and Regulatory Affairs Professionals. It is required to retake every two years.</li>
</ul>
CCRPS Advanced Good Clinical Practice Training
<ul>
 	<li>Entry-level professionals or those transitioning into clinical research roles. This program is suitable for individuals aiming to build foundational skills in trial design, protocol development, and data management.</li>
</ul>
CCRPS Advanced Clinical Research Assistant Training
<ul>
 	<li>Medical professionals such as MDs, IMGs, PharmDs, PhDs, and NPs aiming to transition into roles like Medical Science Liaison (MSL) or Medical Monitor. This program is ideal for those seeking advanced skills in clinical trial oversight, regulatory compliance, and strategic medical communication.</li>
</ul>
CCRPS Advanced Medical Science Liaison and Medical Monitor Training
<ul>
 	<li>Physicians and healthcare professionals with an active medical license or prior experience as Sub-Investigators. This program is tailored for those aiming to lead clinical trials as Principal Investigators, focusing on trial design, sponsor collaboration, and regulatory compliance.</li>
</ul>
CCRPS Advanced Clinical Research Principal Investigator Training
<ul>
 	<li>Entry-level professionals or those transitioning into healthcare administration roles. This program is designed for individuals seeking to develop skills in medical documentation, administrative support, and clinical workflow management.</li>
</ul>
ACMSO Advanced Clinical Medical Scribe and Administrative Assistant Training
<ul>
 	<li>Individuals looking to become a health or life coach or already certified or experienced in health and wellness coaching, looking to expand their expertise into specific niches or a business start up. This program is ideal for those aiming to integrate holistic health strategies with personal development coaching to support clients in achieving both health and life goals.</li>
 	<li>ANHCO Advanced Dual Health and Life Coach TrainingEntry-level professionals or those with some experience in healthcare administration, aiming to specialize in medical billing and coding. This program is suitable for individuals seeking certification in coding systems like ICD-10, CPT, and HCPCS, and those looking to advance in healthcare data management roles.</li>
</ul>
AMBCI Advanced Medical Billing and Coding Training
<ul>
 	<li>Professionals with at least a bachelor's degree looking to expand into project management as well as professionals with foundational project management experience or certifications, such as PMP, looking to deepen their skills in advanced methodologies, risk management, and leadership. This program is tailored for those aiming to lead complex projects across industries.</li>
</ul>
APMIC Advanced Project Management Training
<ul>
 	<li>IT professionals, managers, or cybersecurity specialists seeking advanced training in cybersecurity strategies, risk management, and leadership. This program is ideal for individuals aiming to take on senior roles in cybersecurity management or lead organizational security initiatives.</li>
</ul>
ACSMI Advanced Cybersecurity and Management Training

This field is hidden when viewing the form

Main Website

CAPTCHA

Category: Health & Safety, Healthcare & Pharmaceuticals, Leadership and Management, Science

Description:

CCRPS (Certified Clinical Research Professionals Society): Offering premier clinical research certifications designed for both entry-level and experienced professionals, CCRPS is renowned for its comprehensive curriculum, industry-leading accreditation, and global recognition in clinical research education. Since 2016, CCRPS has trained over 10,000 alumni across our 8 leading programs (ACRAC, ACRCC, APRAC, ARPIC, AGCPC, ACTAC, AMSLC). Per our 2024 Graduate Review, 23% of Alumni Landed Managerial or Higher Level Roles within 4 Years. Featuring accreditations by ACCRE, CPD, PIMED (for CME), and multiple partnerships. Led by Brian Achille, Morgan Hess, John Vinil, Dr.Juan Albano, and several instructors across 8 programs.

ACMSO (Advanced Clinical Medical Scribe Organization): Specializing in medical scribe and Certified Medical Administrative Assistant (CMAA) training, ACMSO provides an industry-standard, interactive online learning environment tailored specifically to aspiring healthcare professionals seeking early clinical exposure and robust job placement opportunities. Since 2021, ACMSO has challenged the norm of early scribe training with affordable and cost-effective. Featuring accreditations by CPD and partnership backing by NHA to prepare students for CMAA certification. Led by Dr.Bilal Ahsan.
https://acmso.org
Medical Scribe & CMAA Certification: https://app.acmso.org/courses/medical-scribe-certification

AMBCI (Advanced Medical Billing and Coding Institute): Recognized for its innovative approach, AMBCI delivers in-depth medical billing and coding training designed for practical application, career readiness, and industry certification, significantly enhancing employability and career prospects. Since 2024, AMBCI has risen to be a top option for training by offering multi-specialty and multi-skill education in an easy-to-learn way. Featuring accreditation by CPD. Partnership with NHA to prepare students for CBCS exams and an Official AAPC Training provider to prepare students for CPB + CPC exams. Led by Anthony Brooks.
https://ambci.org
Medical Billing & Coding Certification: https://app.ambci.org/courses/medical-billing-coding-certification

ANHCO (Advanced National Health Coach Organization): ANHCO leads the way in health and life coaching education, delivering an interactive, CPD-accredited curriculum that equips coaches with advanced techniques and evidence-based practices essential for impactful client outcomes and successful coaching careers. Since 2024, ANHCO has bridged learning gaps for coaches by providing a comprehensive curriculum covering over 495 topics in health and life coaching with our evidence-backed, virtual coaching simulations, and with real business start-up support. Accredited by CPD for 495 Hours. Led by Rebecca Ahmed and Dr.Gina Sobrero.
https://anhco.org
Health & Life Coach Certification: https://app.anhco.org/courses/advanced-dual-health-and-life-coach-certification

ACSMI (Advanced Cybersecurity Management Institute): Offering cutting-edge cybersecurity certifications, ACSMI provides learners with comprehensive, scenario-based training designed to meet the critical cybersecurity skills gap, preparing graduates for immediate industry impact and career advancement. Since 2025, ACSMI has introduced one of the most comprehensive formal multi-domain training designed to bring IT and Tech specialists from entry-mid-level into higher roles. Featuring accreditation by CPD. Led by Janero Washington.
https://acsmi.org
Cybersecurity Certification: https://app.acsmi.org/courses/cybersecurity-management-certification

APMIC (Advanced Project Management Institute Certification): APMIC focuses on providing advanced project management training, integrating the latest industry practices with strategic management skills to prepare professionals for complex, high-stakes project environments and leadership roles. Since 2025, APMIC has introduced the first multi-industry project management certification covering over 80 industries, designed to turn project managers into leaders through our simulation-focused approach. Featuring accreditation by CPD and PMI ATP Training Provider Status. Led by Ibrahim Taylor and Dr.Aridnam Sarkar.
https://apmic.org
Project Management Certification: https://app.apmic.org/courses/project-manager-certification

Accredited Activities:

Clinical Research Associate Training

290 Hours – 4 Weeks Agenda
Develop advanced skills for monitoring clinical trial processes and maintaining data integrity across multiple trial specialities and designs.
Understand compliance with FDA and ICH-GCP standards for trial oversight.
Learn site management, risk assessment, and communication with stakeholders.
Online course
Professionals aiming to start or advance their careers as Clinical Research Associates (CRAs). This includes individuals with some clinical research experience or those transitioning from related fields like healthcare or science. The program is designed for those seeking advanced monitoring skills across various trial types and specialities.
https://app.ccrps.org/courses/cra

Clinical Research Coordinator Training

110 Hours – 3 Weeks Agenda
Master participant recruitment, consent processes, and trial documentation.
Understand regulations, ethical considerations, and trial logistics.
Enhance proficiency in data collection and protocol adherence across specialities.
Online course
Aspiring CRCs such as those with a minimum of 2 2-year degree (RN or LPN okay) and some patient experience. As well as Clinical Research Coordinators (CRCs) with experience to bridge knowledge gaps, tailored for professionals looking to enhance their expertise in managing clinical trials, including project management, compliance, and data management.
https://app.ccrps.org/courses/Clinical-Research-Coordinator

Pharmacovigilance and Regulatory Affairs Training

170 Hours – 4 Weeks Agenda
Gain expertise in monitoring and reporting drug safety and adverse reactions.
Learn risk assessment and global compliance standards (FDA, EMA).
Establish communication skills to relay safety data to regulatory bodies.
Online course
Professionals with prior experience in clinical research or healthcare, such as physicians, pharmacists, or regulatory specialists. This program is ideal for those focusing on pharmacovigilance, regulatory compliance, and safety monitoring in multinational clinical trials.
https://app.ccrps.org/courses/pharmacovigilance-certification

Clinical Research Project Manager Training

290 Hours – 4 Weeks Agenda
Acquire leadership for managing clinical trials from initiation to closure.
Understand resource allocation, timeline adherence, and team coordination.
Learn risk mitigation strategies and problem-solving skills.
Online course
Professionals with prior experience in clinical research or project management, such as Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), or those transitioning into leadership roles. This program is ideal for individuals aiming to become Clinical Trial Managers, Research Project Managers, or Clinical Research Leaders.
https://app.ccrps.org/courses/Advanced-Clinical-Research-Project-Manager-Certification

Good Clinical Practice Certification and Training 2025

70 Hours – 1 Week Agenda
Master global guidelines and ethical standards for clinical trials.
Develop detailed knowledge of sponsor and investigator obligations.
Learn proper documentation and reporting practices for trial data, including updates with E6 (R3) for 2025.
Online course
Designed for all professionals desiring to master good clinical practice guidelines to improve ethical and compliant clinical research. This includes all roles in clinical research as well as increased mastery for experienced Clinical Quality Assurance Professionals, Clinical Research Associates, Project Managers, Investigators, Study Coordinators, and Regulatory Affairs Professionals. It is required to retake every two years.
https://app.ccrps.org/courses/ich-gcp

Leading Research Assistant Training Program

114 Hours – 3 Weeks Agenda
Understand trial design basics and sample management tasks.
Learn regulatory documentation techniques and operational support skills.
Develop strong problem-solving capabilities within trial settings.
Online course
Entry-level professionals or those transitioning into clinical research roles. This program is suitable for individuals aiming to build foundational skills in trial design, protocol development, and data management.
https://app.ccrps.org/courses/Clinical-Trials-Assistant-Training

Medical Science Liaison – Medical Monitor Certification

250 Hours – 4 Weeks Agenda
Gain skills in reviewing trial protocols and assessing participant safety across multiple trial specialities and designs.
Learn adverse event management and medical oversight procedures.
Enhance communication with stakeholders to ensure trial efficacy and leadership.
Online course
Medical professionals such as MDs, IMGs, PharmDs, PhDs, and NPs are aiming to transition into roles like Medical Science Liaison (MSL) or Medical Monitor. This program is ideal for those seeking advanced skills in clinical trial oversight, regulatory compliance, and strategic medical communication.
https://app.ccrps.org/courses/medial-monitor-certification

Principal Investigator Certification

179 Hours – 4 Weeks Agenda
Build expertise in leading clinical trials and overseeing participant safety across multiple trial specialities.
Learn protocol design, budget management, and compliance adherence.
Develop leadership and communication for collaboration with sponsors.
Online course
Physicians and healthcare professionals with an active medical license or prior experience as Sub-Investigators. This program is tailored for those aiming to lead clinical trials as Principal Investigators, focusing on trial design, sponsor collaboration, and regulatory compliance.
https://app.ccrps.org/courses/Advanced-Principal-Investigator-Physician-Certification

Who Should Attend:

Professionals aiming to start or advance their careers as Clinical Research Associates (CRAs). This includes individuals with some clinical research experience or those transitioning from related fields like healthcare or science. The program is designed for those seeking advanced monitoring skills across various trial types and specialities.

CCRPS Advanced Clinical Research Associate Training

Aspiring CRCs such as those with a minimum of 2 2-year degree (RN or LPN okay) and some patient experience. As well as Clinical Research Coordinators (CRCs) with experience to bridge knowledge gaps, tailored for professionals looking to enhance their expertise in managing clinical trials, including project management, compliance, and data management.

CCRPS Advanced Clinical Research Coordinator Training

Professionals with prior experience in clinical research or healthcare, such as physicians, pharmacists, or regulatory specialists. This program is ideal for those focusing on pharmacovigilance, regulatory compliance, and safety monitoring in multinational clinical trials.

CCRPS Advanced Pharmacovigilance and Regulatory Affairs Training

Professionals with prior experience in clinical research or project management, such as Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), or those transitioning into leadership roles. This program is ideal for individuals aiming to become Clinical Trial Managers, Research Project Managers, or Clinical Research Leaders.

CCRPS Advanced Clinical Research Project Manager Training

Designed for all professionals desiring to master good clinical practice guidelines to improve ethical and compliant clinical research. This includes all roles in clinical research as well as increased mastery for experienced Clinical Quality Assurance Professionals, Clinical Research Associates, Project Managers, Investigators, Study Coordinators, and Regulatory Affairs Professionals. It is required to retake every two years.

CCRPS Advanced Good Clinical Practice Training

Entry-level professionals or those transitioning into clinical research roles. This program is suitable for individuals aiming to build foundational skills in trial design, protocol development, and data management.

CCRPS Advanced Clinical Research Assistant Training

Medical professionals such as MDs, IMGs, PharmDs, PhDs, and NPs aiming to transition into roles like Medical Science Liaison (MSL) or Medical Monitor. This program is ideal for those seeking advanced skills in clinical trial oversight, regulatory compliance, and strategic medical communication.

CCRPS Advanced Medical Science Liaison and Medical Monitor Training

Physicians and healthcare professionals with an active medical license or prior experience as Sub-Investigators. This program is tailored for those aiming to lead clinical trials as Principal Investigators, focusing on trial design, sponsor collaboration, and regulatory compliance.

CCRPS Advanced Clinical Research Principal Investigator Training

Entry-level professionals or those transitioning into healthcare administration roles. This program is designed for individuals seeking to develop skills in medical documentation, administrative support, and clinical workflow management.

ACMSO Advanced Clinical Medical Scribe and Administrative Assistant Training

Individuals looking to become a health or life coach or already certified or experienced in health and wellness coaching, looking to expand their expertise into specific niches or a business start up. This program is ideal for those aiming to integrate holistic health strategies with personal development coaching to support clients in achieving both health and life goals.
ANHCO Advanced Dual Health and Life Coach TrainingEntry-level professionals or those with some experience in healthcare administration, aiming to specialize in medical billing and coding. This program is suitable for individuals seeking certification in coding systems like ICD-10, CPT, and HCPCS, and those looking to advance in healthcare data management roles.

AMBCI Advanced Medical Billing and Coding Training

Professionals with at least a bachelor’s degree looking to expand into project management as well as professionals with foundational project management experience or certifications, such as PMP, looking to deepen their skills in advanced methodologies, risk management, and leadership. This program is tailored for those aiming to lead complex projects across industries.

APMIC Advanced Project Management Training

IT professionals, managers, or cybersecurity specialists seeking advanced training in cybersecurity strategies, risk management, and leadership. This program is ideal for individuals aiming to take on senior roles in cybersecurity management or lead organizational security initiatives.

ACSMI Advanced Cybersecurity and Management Training

Further Information:

https://www.ccrps.org