Post-Graduate Certificate in Clinical Trials

This introductory course will orient you to the drug development process in general and the clinical research function in particular. Pharmaceutical drug development will be used as a model. Some exposure will be provided to the development of medical devices and biologics. You will gain an appreciation of the basic concepts in clinical research, such as the various types of clinical trial designs, trial phases, process of randomization, blinding, study start up, clinical trial monitoring, project management, pharmacovigilance, data management and biometrics.

13 Classes

39 Hours

Schedule

January 11 to February 24, 2027

Classes TBA

The objective of this course is to provide you with an understanding of the regulations and ethical principles that govern the conduct of clinical research, as well as their practical application in clinical trials. This course covers the historical rationale for regulatory oversight, major developments of guidelines, and the regulations that apply to the conduct of clinical trials.

13 Classes

39 Hours

Schedule

January 12 to February 23, 2027

Classes TBA

This course will provide you with sound knowledge of key clinical trial design principles, including how to design a protocol and other important aspects of a clinical trial. Today’s healthcare industry is focused on following protocol on designing studies that answer important questions that advance the practice of medicine. This course has been developed to help you effectively navigate important decisions typically faced by clinical researchers when designing and planning clinical studies.

13 Classes

39 Hours

Schedule

March 08 to April 19, 2027

Classes TBA

We will focus on the day-to-day operations of leading a clinical trial. You will gain applied knowledge in financial management, essential documents, recruitment, data management and strategies for safety reporting. Additionally, you will acquire practical experience developing study start-up plans, recruitment and retention plans, and site budgets. Upon completion, you will possess the necessary skills needed to execute clinical research project activities to meet recruitment targets and to deliver high quality data on time and within study budget according to regulatory requirements.

13 Classes

39 Hours

Schedule

March 09 to April 20, 2027

Classes TBA

We will examine oversight mechanisms in clinical research operations, including monitoring, audits, and inspections, as well as safety, medical, and data oversight. The primary aim of this course is to empower you with the knowledge and practical skills sets required for end-to-end monitoring activities. You will gain valuable knowledge of monitoring practices, which are essential to clinical trial conduct and management.

13 Classes

39 Hours

Schedule

May 03 to June 16, 2027

Classes TBA

This comprehensive course equips clinical research professionals with cutting-edge data management skills for today's digitized trial environment. Combining traditional methodologies with emerging technologies, students gain expertise in electronic data systems and innovative data collection approaches that drive trial efficiency and quality.

13 Classes

39 Hours

Schedule

May 04 to June 15, 2027

Classes TBA

Throughout this course, you will engage in Clinical Observation, guided by industry experts. Leveraging a problem-based learning methodology, participants will translate their observations to scenarios that emulate typical events at various stages of clinical trials or studies. The course will place particular emphasis on analyzing the multifaceted roles involved in Clinical Trials, thereby facilitating students' exploration of potential career paths they may wish to pursue post-graduation.

13 Classes

39 Hours

Schedule

July 05 to August 18, 2027

Classes TBA

After the completion of the first seven courses and all of your applied learning assignments, this course is intended to further simulate real-world experience by combining all previous learnings to an applied clinical research management simulation. You will leverage all your knowledge, assignments and experiences to date to further develop your competencies in critical thinking and problem solving, teamwork and collaboration, as well as agility and adaptability, to ensure the successful execution of clinical trials. Taking the hands-on experience to the next level, you will be ready to begin working the field and add immediate value to any clinical research team.

13 Classes

39 Hours

Schedule

July 06 to August 17, 2027

Classes TBA

This introductory course will orient you to the drug development process in general and the clinical research function in particular. Pharmaceutical drug development will be used as a model. Some exposure will be provided to the development of medical devices and biologics. You will gain an appreciation of the basic concepts in clinical research, such as the various types of clinical trial designs, trial phases, process of randomization, blinding, study start up, clinical trial monitoring, project management, pharmacovigilance, data management and biometrics.

13 Classes

39 Hours

Schedule

January 11 to February 24, 2027

Classes TBA

The objective of this course is to provide you with an understanding of the regulations and ethical principles that govern the conduct of clinical research, as well as their practical application in clinical trials. This course covers the historical rationale for regulatory oversight, major developments of guidelines, and the regulations that apply to the conduct of clinical trials.

13 Classes

39 Hours

Schedule

January 12 to February 23, 2027

Classes TBA

This course will provide you with sound knowledge of key clinical trial design principles, including how to design a protocol and other important aspects of a clinical trial. Today’s healthcare industry is focused on following protocol on designing studies that answer important questions that advance the practice of medicine. This course has been developed to help you effectively navigate important decisions typically faced by clinical researchers when designing and planning clinical studies.

13 Classes

39 Hours

Schedule

March 08 to April 19, 2027

Classes TBA

We will focus on the day-to-day operations of leading a clinical trial. You will gain applied knowledge in financial management, essential documents, recruitment, data management and strategies for safety reporting. Additionally, you will acquire practical experience developing study start-up plans, recruitment and retention plans, and site budgets. Upon completion, you will possess the necessary skills needed to execute clinical research project activities to meet recruitment targets and to deliver high quality data on time and within study budget according to regulatory requirements.

13 Classes

39 Hours

Schedule

March 09 to April 20, 2027

Classes TBA

We will examine oversight mechanisms in clinical research operations, including monitoring, audits, and inspections, as well as safety, medical, and data oversight. The primary aim of this course is to empower you with the knowledge and practical skills sets required for end-to-end monitoring activities. You will gain valuable knowledge of monitoring practices, which are essential to clinical trial conduct and management.

13 Classes

39 Hours

Schedule

May 03 to June 16, 2027

Classes TBA

This comprehensive course equips clinical research professionals with cutting-edge data management skills for today's digitized trial environment. Combining traditional methodologies with emerging technologies, students gain expertise in electronic data systems and innovative data collection approaches that drive trial efficiency and quality.

13 Classes

39 Hours

Schedule

May 04 to June 15, 2027

Classes TBA

Throughout this course, you will engage in Clinical Observation, guided by industry experts. Leveraging a problem-based learning methodology, participants will translate their observations to scenarios that emulate typical events at various stages of clinical trials or studies. The course will place particular emphasis on analyzing the multifaceted roles involved in Clinical Trials, thereby facilitating students' exploration of potential career paths they may wish to pursue post-graduation.

13 Classes

39 Hours

Schedule

July 05 to August 18, 2027

Classes TBA

After the completion of the first seven courses and all of your applied learning assignments, this course is intended to further simulate real-world experience by combining all previous learnings to an applied clinical research management simulation. You will leverage all your knowledge, assignments and experiences to date to further develop your competencies in critical thinking and problem solving, teamwork and collaboration, as well as agility and adaptability, to ensure the successful execution of clinical trials. Taking the hands-on experience to the next level, you will be ready to begin working the field and add immediate value to any clinical research team.

13 Classes

39 Hours

Schedule

July 06 to August 17, 2027

Classes TBA

This introductory course will orient you to the drug development process in general and the clinical research function in particular. Pharmaceutical drug development will be used as a model. Some exposure will be provided to the development of medical devices and biologics. You will gain an appreciation of the basic concepts in clinical research, such as the various types of clinical trial designs, trial phases, process of randomization, blinding, study start up, clinical trial monitoring, project management, pharmacovigilance, data management and biometrics.

13 Classes

39 Hours

Schedule

September 13 to October 27, 2027

Classes Mon,Wed 6:00 PM-9:00 PM (13 Sep 2027 to 27 Oct 2027)

The objective of this course is to provide you with an understanding of the regulations and ethical principles that govern the conduct of clinical research, as well as their practical application in clinical trials. This course covers the historical rationale for regulatory oversight, major developments of guidelines, and the regulations that apply to the conduct of clinical trials.

13 Classes

39 Hours

Schedule

September 14 to October 26, 2027

Classes Tue,Thu 6:00 PM-9:00 PM (14 Sep 2027 to 26 Oct 2027)

This course will provide you with sound knowledge of key clinical trial design principles, including how to design a protocol and other important aspects of a clinical trial. Today’s healthcare industry is focused on following protocol on designing studies that answer important questions that advance the practice of medicine. This course has been developed to help you effectively navigate important decisions typically faced by clinical researchers when designing and planning clinical studies.

13 Classes

39 Hours

Schedule

November 01 to December 13, 2027

Classes Mon,Wed 6:00 PM-9:00 PM (01 Nov 2027 to 13 Dec 2027)

We will focus on the day-to-day operations of leading a clinical trial. You will gain applied knowledge in financial management, essential documents, recruitment, data management and strategies for safety reporting. Additionally, you will acquire practical experience developing study start-up plans, recruitment and retention plans, and site budgets. Upon completion, you will possess the necessary skills needed to execute clinical research project activities to meet recruitment targets and to deliver high quality data on time and within study budget according to regulatory requirements.

13 Classes

39 Hours

Schedule

November 02 to December 14, 2027

Classes Tue,Thu 6:00 PM-9:00 PM (02 Nov 2027 to 14 Dec 2027)

This comprehensive course equips clinical research professionals with cutting-edge data management skills for today's digitized trial environment. Combining traditional methodologies with emerging technologies, students gain expertise in electronic data systems and innovative data collection approaches that drive trial efficiency and quality.

13 Classes

39 Hours

Schedule

January 04 to February 15, 2028

Classes Tue,Thu 6:00 PM-9:00 PM (04 Jan 2028 to 15 Feb 2028)

We will examine oversight mechanisms in clinical research operations, including monitoring, audits, and inspections, as well as safety, medical, and data oversight. The primary aim of this course is to empower you with the knowledge and practical skills sets required for end-to-end monitoring activities. You will gain valuable knowledge of monitoring practices, which are essential to clinical trial conduct and management.

13 Classes

39 Hours

Schedule

January 05 to February 16, 2028

Classes Mon,Wed 6:00 PM-9:00 PM (05 Jan 2028 to 16 Feb 2028)

Throughout this course, you will engage in Clinical Observation, guided by industry experts. Leveraging a problem-based learning methodology, participants will translate their observations to scenarios that emulate typical events at various stages of clinical trials or studies. The course will place particular emphasis on analyzing the multifaceted roles involved in Clinical Trials, thereby facilitating students' exploration of potential career paths they may wish to pursue post-graduation.

13 Classes

39 Hours

Schedule

February 28 to April 10, 2028

Classes Mon,Wed 6:00 PM-9:00 PM (28 Feb 2028 to 10 Apr 2028) ()

After the completion of the first seven courses and all of your applied learning assignments, this course is intended to further simulate real-world experience by combining all previous learnings to an applied clinical research management simulation. You will leverage all your knowledge, assignments and experiences to date to further develop your competencies in critical thinking and problem solving, teamwork and collaboration, as well as agility and adaptability, to ensure the successful execution of clinical trials. Taking the hands-on experience to the next level, you will be ready to begin working the field and add immediate value to any clinical research team.

13 Classes

39 Hours

Schedule

February 29 to April 11, 2028

Classes Tue,Thu 6:00 PM-9:00 PM (29 Feb 2028 to 11 Apr 2028)

This introductory course will orient you to the drug development process in general and the clinical research function in particular. Pharmaceutical drug development will be used as a model. Some exposure will be provided to the development of medical devices and biologics. You will gain an appreciation of the basic concepts in clinical research, such as the various types of clinical trial designs, trial phases, process of randomization, blinding, study start up, clinical trial monitoring, project management, pharmacovigilance, data management and biometrics.

13 Classes

39 Hours

Schedule

September 13 to October 27, 2027

Classes Mon,Wed 6:00 PM-9:00 PM (13 Sep 2027 to 27 Oct 2027)

The objective of this course is to provide you with an understanding of the regulations and ethical principles that govern the conduct of clinical research, as well as their practical application in clinical trials. This course covers the historical rationale for regulatory oversight, major developments of guidelines, and the regulations that apply to the conduct of clinical trials.

13 Classes

39 Hours

Schedule

September 14 to October 26, 2027

Classes Tue,Thu 6:00 PM-9:00 PM (14 Sep 2027 to 26 Oct 2027)

This course will provide you with sound knowledge of key clinical trial design principles, including how to design a protocol and other important aspects of a clinical trial. Today’s healthcare industry is focused on following protocol on designing studies that answer important questions that advance the practice of medicine. This course has been developed to help you effectively navigate important decisions typically faced by clinical researchers when designing and planning clinical studies.

13 Classes

39 Hours

Schedule

November 01 to December 13, 2027

Classes Mon,Wed 6:00 PM-9:00 PM (01 Nov 2027 to 13 Dec 2027)

We will focus on the day-to-day operations of leading a clinical trial. You will gain applied knowledge in financial management, essential documents, recruitment, data management and strategies for safety reporting. Additionally, you will acquire practical experience developing study start-up plans, recruitment and retention plans, and site budgets. Upon completion, you will possess the necessary skills needed to execute clinical research project activities to meet recruitment targets and to deliver high quality data on time and within study budget according to regulatory requirements.

13 Classes

39 Hours

Schedule

November 02 to December 14, 2027

Classes Tue,Thu 6:00 PM-9:00 PM (02 Nov 2027 to 14 Dec 2027)

This comprehensive course equips clinical research professionals with cutting-edge data management skills for today's digitized trial environment. Combining traditional methodologies with emerging technologies, students gain expertise in electronic data systems and innovative data collection approaches that drive trial efficiency and quality.

13 Classes

39 Hours

Schedule

January 04 to February 15, 2028

Classes Tue,Thu 6:00 PM-9:00 PM (04 Jan 2028 to 15 Feb 2028)

We will examine oversight mechanisms in clinical research operations, including monitoring, audits, and inspections, as well as safety, medical, and data oversight. The primary aim of this course is to empower you with the knowledge and practical skills sets required for end-to-end monitoring activities. You will gain valuable knowledge of monitoring practices, which are essential to clinical trial conduct and management.

13 Classes

39 Hours

Schedule

January 05 to February 16, 2028

Classes Mon,Wed 6:00 PM-9:00 PM (05 Jan 2028 to 16 Feb 2028)

Throughout this course, you will engage in Clinical Observation, guided by industry experts. Leveraging a problem-based learning methodology, participants will translate their observations to scenarios that emulate typical events at various stages of clinical trials or studies. The course will place particular emphasis on analyzing the multifaceted roles involved in Clinical Trials, thereby facilitating students' exploration of potential career paths they may wish to pursue post-graduation.

13 Classes

39 Hours

Schedule

February 28 to April 10, 2028

Classes Mon,Wed 6:00 PM-9:00 PM (28 Feb 2028 to 10 Apr 2028) ()

After the completion of the first seven courses and all of your applied learning assignments, this course is intended to further simulate real-world experience by combining all previous learnings to an applied clinical research management simulation. You will leverage all your knowledge, assignments and experiences to date to further develop your competencies in critical thinking and problem solving, teamwork and collaboration, as well as agility and adaptability, to ensure the successful execution of clinical trials. Taking the hands-on experience to the next level, you will be ready to begin working the field and add immediate value to any clinical research team.

13 Classes

39 Hours

Schedule

February 29 to April 11, 2028

Classes Tue,Thu 6:00 PM-9:00 PM (29 Feb 2028 to 11 Apr 2028)