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Top 11 Clinical Trial Manager Certifications

Photo of Brenna Goyette
Brenna Goyette
Certified Professional Resume Writer, Career Expert

Updated 17 min read

Certifications are important for a clinical trial manager in the job market because they demonstrate to employers that the individual has a high level of knowledge and experience in the field. Certifications can help differentiate an individual from other applicants who may have similar qualifications but lack the specialized expertise provided by such certifications. Additionally, certifications provide assurance to employers that the individual is competent in their knowledge and skills, which is important when managing complex projects. Finally, certifications can open doors to higher-level positions and job opportunities that may otherwise be out of reach due to lack of prior experience.

The purpose of this article is to provide an overview of the most beneficial certifications for Clinical Trial Managers and how they can enhance their career prospects.

What are Clinical Trial Manager Certifications?

Clinical trial manager certification is an industry-recognized credential that verifies a professional’s knowledge and experience in the field of clinical trials management. Clinical trial managers are responsible for overseeing the operational aspects of clinical trials, including developing protocols, setting up clinical trial sites, monitoring data, and ensuring compliance with regulatory standards. The certification process ensures that professionals have a comprehensive understanding of the principles and practices involved in managing clinical trials.

Having a clinical trial manager certification can help individuals stand out from other applicants when applying for jobs or promotions in the field. It also demonstrates to employers that an individual has been trained in best practices related to running successful clinical trials, which can give them a competitive edge over those who don’t have this type of certification. Additionally, having this credential can open up opportunities for networking with other certified clinical trial managers who may be able to provide valuable insights into the industry or offer advice on career advancement. Ultimately, having a clinical trial manager certification can help individuals gain recognition as experts in their field and advance their careers.

Pro Tip: Take advantage of online clinical trial manager certification programs to stay up-to-date on the latest industry trends and best practices. Doing so will help you stay competitive in the job market and give you a better understanding of the clinical trial process.

Related: What does a Clinical Trial Manager do?

Top 11 Clinical Trial Manager Certifications

Here’s our list of the best certifications available to Clinical Trial Managers today.

1. Certified Clinical Research Professional (CCRP)

Certified Clinical Research Professional (CCRP) is a professional certification program for individuals working in the clinical research field. It is awarded by the Association of Clinical Research Professionals (ACRP) and is recognized as an international benchmark of excellence.

To become a CCRP, applicants must meet certain educational, experience, and ethical requirements. Applicants must have at least a Bachelor’s degree in a related field such as life sciences or healthcare. They must also have at least two years of full-time clinical research experience or its equivalent in part-time work. Additionally, applicants must pass an ACRP-administered exam to demonstrate their knowledge and understanding of the principles and practices of clinical research.

The process to become a CCRP typically takes about six months from start to finish. After meeting the eligibility requirements, applicants must register for the exam with ACRP and submit all required documentation. Once approved, they can select an available testing date and location that works for them. The exam consists of 200 multiple choice questions which are divided into four sections: Regulatory Affairs & Good Clinical Practices; Clinical Operations & Project Management; Data Management & Statistics; and Ethics & Professionalism.

The cost to become a CCRP is currently $595 USD for ACRP members and $795 USD for non-members (which includes one year of membership). This fee covers the application fee, exam registration fee, study materials, and access to online practice exams.

2. Certified Clinical Trials Professional (CCTP)

A Certified Clinical Trials Professional (CCTP) is a professional designation that recognizes individuals who have demonstrated expertise in the field of clinical trials. This certification is offered by the Association of Clinical Research Professionals (ACRP). It is designed to recognize and validate the knowledge, skills, and experience of clinical research professionals.

To become certified, applicants must meet certain eligibility requirements, including having at least two years of full-time clinical research experience or equivalent part-time experience within the last five years. They must also pass an exam administered by ACRP. The exam consists of 150 multiple-choice questions covering topics such as ethics and regulations, study design and management, data management, safety monitoring, and quality assurance.

The cost for the CCTP certification exam is $495 for members of ACRP and $595 for non-members. The certification must be renewed every three years by completing continuing education activities approved by ACRP.

3. Certified Clinical Trial Administrator (CCTA)

Certified Clinical Trial Administrator (CCTA) is a professional certification offered by the Society of Clinical Research Associates (SOCRA). It is designed to recognize individuals who have demonstrated knowledge and experience in clinical research administration. The CCTA credential is awarded to those who meet the criteria established by SOCRA, including passing an examination.

The CCTA exam consists of multiple choice questions that cover topics related to clinical research administration such as regulatory requirements, budgeting and finance, project management, data management, and ethics. It typically takes about two hours to complete the exam.

To be eligible for the CCTA certification, applicants must have at least three years of full-time experience in clinical research administration within the last five years. They must also submit proof of education or training in clinical research administration or a related field.

The cost for taking the CCTA exam is $400 for SOCRA members and $500 for non-members.

4. Certified Clinical Research Associate (CCRA)

A Certified Clinical Research Associate (CCRA) is a professional certification for individuals who are involved in the clinical research process. This certification demonstrates that an individual has the knowledge and experience to work in the field of clinical research.

The CCRA certification is offered by the Association of Clinical Research Professionals (ACRP). To become certified, applicants must have a minimum of two years of full-time experience in clinical research or related activities, such as data management or regulatory affairs. Additionally, applicants must pass an exam administered by ACRP. The exam consists of multiple-choice questions and covers topics such as Good Clinical Practice, regulatory compliance, ethics and data management.

It typically takes six months to one year to complete the application process and obtain the CCRA certification. During this time, applicants must submit their applications, complete any required training courses, and take and pass the exam.

The cost of obtaining a CCRA certification varies depending on whether you are a member of ACRP or not. For non-members, it costs $1,495 to apply for the exam; if you are an ACRP member, it costs $795 to apply for the exam.

5. Certified Clinical Data Manager (CCDM)

Certified Clinical Data Manager (CCDM) is a certification program designed to recognize and validate the knowledge, skills, and abilities of clinical data managers. The CCDM certification is administered by the Association of Clinical Research Professionals (ACRP).

The CCDM exam consists of 150 multiple-choice questions covering topics such as data management processes, database design and development, clinical trial regulations and guidelines, medical terminology, statistics and analytics, quality assurance/quality control procedures, and project management. The exam takes approximately 3 hours to complete.

In order to become certified as a CCDM, individuals must have at least two years of experience in clinical data management or related fields. They must also pass the CCDM exam with a score of 70% or higher.

The cost of the CCDM exam is $495 USD for ACRP members and $595 USD for non-members. There are also additional fees for re-testing ($200 USD) and late registration ($50 USD).

6. Certified Quality Assurance Auditor (CQAA)

A Certified Quality Assurance Auditor (CQAA) is a professional designation that recognizes an individual’s expertise in the field of quality assurance. The CQAA certification demonstrates a commitment to quality assurance and provides employers with a way to identify qualified professionals who understand the principles of quality assurance and can effectively audit processes, products, and services.

The CQAA certification is offered by the American Society for Quality (ASQ). To become certified, applicants must pass an exam that covers topics such as auditing principles, quality management systems, process improvement techniques, and problem-solving skills.

The exam takes approximately four hours to complete and consists of multiple choice questions. The cost of the exam is $395 USD for ASQ members and $495 USD for non-members. Additionally, applicants must have at least three years of experience in quality assurance or related fields to be eligible for the exam.

7. Certified Regulatory Affairs Professional (CRAP)

Certified Regulatory Affairs Professional (CRAP) is a professional certification program offered by the Regulatory Affairs Professionals Society (RAPS). It is designed to recognize individuals who have achieved a high level of proficiency in the field of regulatory affairs. The CRAP program provides a comprehensive examination that tests knowledge and skills related to regulatory compliance, product registration, and other areas of regulatory affairs.

It typically takes about six months to complete the CRAP program. The first step is to become familiar with the RAPS Code of Ethics and Standards of Practice as well as the RAPS Certification Examination Handbook. Once you have reviewed these documents, you can then apply for the exam by submitting an application form and paying the required fee.

Once your application has been approved, you will be sent a study guide that outlines all of the topics covered by the exam. You will then need to study for the exam using this guide and any other materials provided by RAPS. After completing your studies, you can then register for and take the exam at an authorized testing center.

The cost of taking the CRAP exam varies depending on where you take it and if you are taking it online or in-person. Generally speaking, however, it costs around $400-$500 USD to take the exam online or $600-$700 USD to take it in-person at an authorized testing center.

8. Good Clinical Practice Certification (GCP)

Good Clinical Practice (GCP) Certification is a certification program that provides assurance to the public that clinical research studies are conducted according to international standards. It is designed to protect the rights, safety and well-being of human participants involved in research studies and ensure the integrity of data generated from such studies. GCP Certification is required for any researcher conducting clinical trials or other forms of medical research involving human subjects.

GCP Certification typically takes about 6-8 weeks to complete, depending on the individual's experience level and availability of study materials. To get GCP Certified, individuals must first complete an online training course and pass a written exam. The cost of GCP Certification varies depending on the provider, but generally ranges from $200-$400 USD.

In addition to completing the training course and passing the exam, individuals must also demonstrate their knowledge by participating in a practical exercise or case study. This exercise may involve reviewing a clinical trial protocol or designing a trial plan for a particular disease or condition. Once all requirements have been met, applicants will receive their GCP Certification.

9. Project Management Professional Certification (PMP)

Project Management Professional Certification (PMP) is a globally recognized certification for project managers. It is offered by the Project Management Institute (PMI), a non-profit organization that sets standards for project management. The PMP certification is designed to recognize individuals who have demonstrated their knowledge, skills, and experience in leading and managing projects.

The PMP certification process consists of four steps: completing an application, passing an exam, meeting the experience requirements, and agreeing to adhere to the PMI Code of Ethics. To be eligible for the PMP exam, applicants must have either a secondary degree (high school diploma or equivalent) plus at least five years of professional project management experience with 7500 hours leading and directing projects; or a four-year degree plus at least three years of professional project management experience with 4500 hours leading and directing projects.

The PMP exam consists of 200 multiple-choice questions that test your knowledge on five major domains: Initiating the Project, Planning the Project, Executing the Project, Monitoring & Controlling the Project, and Closing the Project. The total time allotted for taking the exam is four hours. You must score at least 61% correct answers in order to pass.

The cost of obtaining a PMP certification varies depending on whether you are a member or non-member of PMI. For members it costs $405 USD while for non-members it costs $555 USD. The cost includes access to online learning materials as well as two attempts at taking the exam within one year from purchase date.

It typically takes about 6 months to prepare for and obtain a PMP certification if you are already familiar with project management concepts and processes. However if you are new to project management it may take up to 12 months or longer depending on your level of commitment and dedication towards studying for the exam.

10. Six Sigma Green Belt Certification

Six Sigma Green Belt Certification is a certification program designed to recognize professionals who have achieved a level of expertise in the application of Six Sigma principles and tools. It demonstrates that an individual has the knowledge and skills necessary to lead improvement projects, analyze data, and identify areas for improvement within an organization.

The Six Sigma Green Belt Certification typically takes between two to three months to complete. To get certified, individuals must first complete a training course, which can be done through an accredited institution or online. After completing the training course, candidates must pass a certification exam to demonstrate their mastery of the material. The cost of the certification exam varies depending on where it is taken, but typically ranges from $200-$300 USD.

To maintain their certification, individuals must participate in continuing education activities related to Six Sigma every three years. This can include attending conferences or workshops, taking additional courses or reading books related to Six Sigma principles and tools.

11. American Society of Clinical Oncology-Certified Oncology Research Professional Certification

The American Society of Clinical Oncology (ASCO) Certified Oncology Research Professional Certification is a professional certification program designed to recognize the knowledge and skills of oncology research professionals. This certification is intended for individuals who are currently working in or are interested in pursuing a career in oncology research. The certification is awarded after successful completion of an exam that assesses the individual’s knowledge and skills related to oncology research.

The ASCO Certified Oncology Research Professional Certification requires applicants to have at least two years of experience in oncology research, including at least one year of direct patient care experience. Applicants must also complete an online application and submit their resume, two letters of recommendation, and a copy of their transcripts. Once accepted into the program, applicants must pass a comprehensive exam that covers topics such as clinical trial design, data management, regulatory compliance, ethics, and quality assurance.

The exam takes approximately four hours to complete and can be taken either online or in person at an authorized testing center. The cost for the exam varies depending on location but typically ranges from $400-$500 USD. Upon successful completion of the exam, applicants will receive their ASCO Certified Oncology Research Professional Certification which is valid for three years before needing to be renewed.

Do You Really Need a Clinical Trial Manager Certificate?

The clinical trial manager certificate is a great way to demonstrate your commitment and knowledge of the clinical trial process. However, it is not necessary for everyone. Whether or not you need such a certificate depends on what kind of job you are looking for and the level of experience you already have in this field.

If you are just starting out in the clinical trial industry and don’t have much experience, then a certificate might be beneficial. It can give you an advantage over other applicants who don’t have any formal training in this area. It also shows employers that you are taking initiative to further your education and stay up-to-date with the latest developments in the field.

On the other hand, if you already have years of experience working as a clinical trial manager then having a certificate may not be as important. Many employers understand that hands-on experience is far more valuable than any formal certification when it comes to managing complex trials.

Ultimately, it is up to each individual to decide whether or not they need a clinical trial manager certificate. If you feel like having one could benefit your career then it may be worth investing in one. Otherwise, focus on gaining more experience and developing your skills through practice and research instead.

Related: Clinical Trial Manager Resume Examples

FAQs About Clinical Trial Manager Certifications

1. What is a Clinical Trial Manager Certification?

Answer: A Clinical Trial Manager Certification is a professional certification that demonstrates an individual’s knowledge and skills in managing clinical trials. It is typically earned by completing a course or program at an accredited university or institution.

2. How long does it take to obtain a Clinical Trial Manager Certification?

Answer: The time required to complete the necessary coursework and obtain the certification varies depending on the program, but it typically takes between 6 months and two years to complete.

3. What are the benefits of obtaining a Clinical Trial Manager Certification?

Answer: Obtaining a Clinical Trial Manager Certification can help individuals demonstrate their expertise in conducting clinical trials, as well as increase their chances for advancement within the field. It also gives them access to specialized resources and networking opportunities with other professionals in the industry.

4. What type of job opportunities are available with a Clinical Trial Manager Certification?

Answer: A Clinical Trial Manager Certification can open up many different job opportunities within the field of clinical research, including positions such as project manager, data manager, study coordinator, and clinical trial consultant.

5. Is there an exam required to obtain a Clinical Trial Manager Certification?

Answer: Yes, most programs require individuals to pass an exam in order to receive their certification. The exams may vary depending on the program, but generally cover topics such as research ethics, regulatory compliance, data management and statistical analysis.

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Brenna Goyette

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Brenna is a certified professional resume writer, career expert, and the content manager of the ResumeCat team. She has a background in corporate recruiting and human resources and has been writing resumes for over 10 years. Brenna has experience in recruiting for tech, finance, and marketing roles and has a passion for helping people find their dream jobs. She creates expert resources to help job seekers write the best resumes and cover letters, land the job, and succeed in the workplace.

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