40 Courses and Certifications

Online Clinical Research Courses & Certifications

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Post Graduate Diploma in Clinical Research

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Certificate

Post Graduate Diploma in Clinical Research

The Post Graduate Diploma In Clinical Research training is a certification course designed to equip students with the comprehensive knowledge and skills necessary for a successful career in the dynamic field of clinical research. This course delves into the detailed processes involved in designing, conducting, monitoring, and managing clinical trials, ensuring that participants gain a profound understanding of the ethical, regulatory, and scientific aspects of clinical research. 

The Post Graduate Diploma In Clinical Research certification by Clini Launch Research Institute explores key topics such as protocol development, data collection and analysis, pharmacovigilance, and regulatory compliance. The course explores several theoretical concepts with practical applications, fostering critical thinking and problem-solving abilities essential for addressing real-world challenges in the pharmaceutical and healthcare industries. 

Read more: Clinical Research Certification Courses

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10 Months
PG Diploma in Advance Clinical research & PVCDM

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Institute of Clinical Research India via Institute of Clinical Research India, Delhi
Certificate

PG Diploma in Advance Clinical research & PVCDM

The PG Diploma in Advance Clinical Research & PVCDM course is a highly sought-after programme within the science fraternity. The course is designed to provide students with job-oriented training in pharmacovigilance and clinical data management. The PG Diploma in Advance Clinical Research & PVCDM certification by ICRI-MAX Hospital offers a unique opportunity for students to study at the multi-specialty Max Hospital in Saket, Delhi. With a sprawling 43-acre campus and over 1,250 beds, Max Hospital provides a hospital environment for students to gain practical exposure to how trials are conducted. 

Students also get the chance to work with eminent doctors who are already a part of clinical trials. The duration of the PG Diploma in Advance Clinical Research & PVCDM certification course is 10 months, during which students will cover a wide range of subjects including clinical research, pharmacology, drug development, regulations, biostatistics, data management, and drug safety. The curriculum is designed to provide industry-based, practical learning, preparing students for successful careers in the field. Successful candidates can land an internship opportunity with Max Hospital, which can lead to job placements.

Also read: Clinical Research Certification Courses

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10 Months
Enquire
Advance Diploma in Clinical Research

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Certificate

Advance Diploma in Clinical Research

The Advanced Diploma In Clinical Research training is a certification course designed to equip aspiring students with the advanced knowledge and skills required to excel in the dynamic field of clinical research. This course goes beyond the fundamentals, delving into intricate aspects of the research process, and ethical considerations. This advanced diploma not only imparts theoretical knowledge but also emphasises practical application through hands-on training and case studies. 

Advanced Diploma In Clinical Research certification by Clini Launch Research Institute provides the students with an in-depth understanding of designing and managing clinical trials, statistical analysis, data management, and reporting methodologies. The programme integrates the latest industry trends, technological advancements, and global best practices, ensuring that students are well-prepared to navigate the complexities of the clinical research landscape. 

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6 Months
89,999
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Certificate

eCourse in Clinical Research Methods

The Clinical Research Methods online course is a four-month program supporting improved clinical examination methodologies. This training empowers candidates to carry out their full-fledged research. Applicants can log in from their personal computers or laptops to learn through the online assessments, lectures, and recommended readings offered throughout the course.

eCourse in Clinical Research Methods certification syllabus integrates self-learning and online lectures with study materials. It divides into four learning modules that cover all aspects of clinical research, taught through a hybrid online learning/teaching technique via a web-based portal. The curriculum covers quantitative and qualitative designs, data management, ethical principles, and thesis reports in a clinical research background. 

The Public Health Foundation of India has developed the course. Dr. Tanica Lyngdoh is an additional professor at the Indian Institute of Public Health, Delhi, and the program coordinator. A final MCQ-based online test will determine the candidate’s eligibility for the course completion certification. Learners will have to pay separately for the course materials and certificate of the Clinical Research Methods training.

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4 Months
9,000
Skills Covered:
Knowledge of healthcare sciences
Certification in Clinical Research

Offered by

Certificate

Certification in Clinical Research

The Certification in Clinical Research is a course designed to equip aspiring professionals with the knowledge and skills essential for success in the dynamic field of clinical research. This course provides a thorough understanding of the fundamental principles, methodologies, and regulatory aspects governing clinical trials and research studies. Students will possess a solid foundation to excel in various roles within the clinical research domain, contributing significantly to advancements in healthcare and medical science.

The Certification in Clinical Research training delves into topics like research ethics, protocol development, data collection and analysis, and Good Clinical Practice (GCP) guidelines. With a focus on the practical application of theoretical concepts, the course incorporates case studies, simulations, and real-world scenarios to ensure a well-rounded learning experience among students. 

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4 Months
What Every Provider Should Know Clinical Fundamentals

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Certificate

What Every Provider Should Know: Clinical Fundamentals

The What Every Provider Should Know: Clinical Fundamentals training spans ten weeks of learning. The course has been created by Stanford University. It is an introductory course, and video transcripts for the online lessons are available too so that it gets easier for the individuals to study. Moreover, this program comes under the discipline of medicine.

Furthermore, the What Every Provider Should Know: Clinical Fundamentals certification syllabus is such that a student can learn at his or her pace and schedule. The concepts are explained in detail through case studies. Also, pupils get to network with each other, which aids them in building a community and applying the concepts during their clinical practice. 

In addition, for the What Every Provider Should Know: Clinical Fundamentals online course, a student needs to allow a bare minimum of four to six hours every week to finish the course successfully. Moreover, you get access to premium quality video lectures, discussion forums, etc. during the course. Designed by EM experts and medicine academicians, the training entails zero prerequisites.

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10 Weeks
Beginner
Free
Skills Covered:
Knowledge of healthcare sciences
Current Regulatory Requirements for Conducting Clinical Trials in India for Investigational New Drugs New Drug

Offered by

CDSA , Central Drugs Standard Control Organisation via Swayam
Certificate

Current Regulatory Requirements For Conducting Clinical Trials In India For Investigational New Drugs/New Drug (Version 3.0)

The Regulatory Requirements for Conducting Clinical Trials programme has been developed by the Clinical Development Services Agency (CDSA) in association with NPTEL and  Central Drugs Standard Control Organisation (CDSCO). It is a prerequisite course if you are interested in conducting clinical trials and involving yourself in developing new drugs. The course will also discuss the latest guidelines and regulations in the New Drugs and Clinical Trials (NDCT) Rules, 2019.

Regulatory Requirements for Conducting Clinical Trials certification is an elective course with a duration of eight weeks. It is a multidisciplinary course that you can access on Swayam, the online learning platform. There are no prerequisites to join this online course. All the course material is available for free. You will also have the chance to study under a reputed group of educators from multiple organisations and institutions.

Regulatory Requirements for Conducting Clinical Trials has an option for certification as well. You need to submit all the assignments and sit for the offline end-of-term exam to obtain it.

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8 Weeks
Free
Skills Covered:
Knowledge of healthcare sciences
Introduction to Clinical Data

Offered by

Certificate

Introduction to Clinical Data

Introduction to Clinical Data is an online course offered by the Stanford University School of Medicine which is accredited by the Accreditation Council for Continuing Medical Education (ACCME). The programme designed for beginner-level students will discuss the clinical data broadly. 

Introduction to Clinical Data Certification Syllabus will walk the learners through ethical medical data mining and the elements of bias and fairness in clinical and healthcare data in making decisions about the care for the patients. By taking the programme, the students will be able to learn to build datasets and clean the clinical doubts and queries with the help of computational procedures. 

Introduction to Clinical Data Certification Course, offered by Coursera, is completely designed for the beginner-level learner with flexible deadlines. Introduction to Clinical Data Certification by Coursera, tutored by Nigam Shah, David Magnus, and Steven Bagley, is the second in the five courses of AI in Healthcare Specialization. 

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8 Weeks
Beginner
6,638
Skills Covered:
Knowledge of Data mining
Certificate

Improving Healthcare Through Clinical Research

Improving Healthcare Through Clinical Research certification is an online course where certificates have been jointly given both by FutureLearn, the University of Leeds, and the National Institute for Health Research. From this 4 hours course which is held weekly, the candidates are able to explore the benefits, and challenges of modern healthcare with respect to clinical research.

Anything that is done for the healthcare sector has to be discovered first and then tested thoroughly before it can be used for practice. Improving Healthcare Through Clinical Research certification syllabus allows the students to learn through case studies, and also investigate what kind of research takes place for doing treatment of deadly diseases like cancer, and dementia.

With Improving Healthcare Through Clinical Research, candidates can raise ethical questions on the research process, and even learn how the research team’s members, participants, and academics are responsible for contributing to this process of clinical discovery.

Also Read:Health Informatics for better and safer healthcare

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4 Weeks
Beginner
Free
Skills Covered:
Knowledge of healthcare sciences
Design and Interpretation of Clinical Trials

Offered by

Certificate

Design and Interpretation of Clinical Trials

The course titled Design and Interpretation of Clinical Trials introduces the learner to clinical trials and how they are carried out. Simply put, clinical trials are experiments that test new ways to prevent or treat diseases in people. These ways can be drugs, devices, surgeries, and so on. These experiments are carried out to test out treatments, medicines, or procedures to see how they affect their subjects.

The Design and Interpretation of Clinical Trials certification by Coursera will provide an in-depth understanding of the principles behind the design of randomised clinical trials. Through the course, the learner will be introduced to the process of clinical trials, and eventually, they will learn how to analyse and interpret these clinical trials. The course includes approximately 10 hours of video lessons and reading material.

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3 Weeks
Free
Clinical Trials Data Management and Quality Assurance

Offered by

Certificate

Clinical Trials Data Management and Quality Assurance

Clinical Trials Data Management and Quality Assurance is an online certification course designed to enable students to understand how to collect the data gathered during trials. The online course teaches students ways to avoid mistakes through quality assurance practices. Clinical Trials Data Management and Quality Assurance certification by Coursera enables the student to identify the right collection instruments, systems, and measures to protect the integrity of trial data.

Clinical Trials Data Management and Quality Assurance training covers how to assemble and share clinical trial data and explains how to conduct statistical performance monitoring. The Clinical Trials Data Management and Quality Assurance online course consists of ways to manage treatment interventions and gain technical expertise in data management to attain prominence in the field.

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3 Weeks
Beginner
4,117
Clinical Trials Management and Advanced Operations

Offered by

Certificate

Clinical Trials Management and Advanced Operations

Clinical Trials Management and Advanced Operations is an online certification course designed to familiarise students with the advanced elements involved in managing clinical trials. The online course teaches students the fundamental skills to implement best practices throughout the trial process. The Clinical Trials Management and Advanced Operations certification course is offered by Coursera and is a part of the Clinical Trials Operations Specialization. 

The Clinical Trials Management and Advanced Operations training covers how to plan, manage, anticipate clinical trials and how systematic review and meta-analysis is used to mix evidence from multiple sources. The Clinical Trials Management and Advanced Operations online course helps students gain a firm understanding when it comes to practising advanced operations in clinical trials.

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3 Weeks
Beginner
4,117
Design and Conduct of Clinical Trials

Offered by

Certificate

Design and Conduct of Clinical Trials

Design and Conduct of Clinical Trials is an online certification course designed to understand the fundamental concepts related to the conduct of clinical trials. The online course aims to teach students the essential skills required to carry out clinical trials. The Design and Conduct of Clinical Trials Certification is offered by Coursera and is a part of the Clinical Trials Operation Specialization. 

The Design and Conduct of Clinical Trials training covers strategies to conduct clinical trials, mask treatments, testing hypotheses, randomize participants. Through this online certification course, students will be familiar with the guiding principles and the essential skills to evaluate and select clinical trial designs. The Design and Conduct of Clinical Trials online course guides students regarding the important technical necessities to focus on while designing and conducting clinical trials.

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3 Weeks
Beginner
4,117
Skills Covered:
Analytical skills
Clinical Trials Analysis Monitoring and Presentation

Offered by

Certificate

Clinical Trials Analysis, Monitoring, and Presentation

Clinical Trials Analysis, Monitoring, and Presentation is an online certification course aimed at teaching students the advanced operational skills needed to run a successful clinical trial. The online course is designed to familiarise students with how to calculate clinical trial sample size to form a suitable trial design and outcome measures. The Clinical Trials Analysis, Monitoring, and Presentation certification is offered by Coursera, which is a part of the Clinical Trials Operations Specialization. 

The Clinical Trials Analysis, Monitoring, and Presentation training covers statistical concepts to monitor a trial for safety and efficacy. Through this online certification course, students will be able to learn practical concepts when it comes to analysing, monitoring and presenting clinical trial data. The Clinical Trials Analysis, Monitoring, and Presentation online course points out the role of data and management in clinical trials.

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3 Weeks
Beginner
4,117
Skills Covered:
Communication skills
Faster Together Enhancing the Recruitment of Minorities in Clinical Trials

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Certificate

Faster Together, Enhancing the Recruitment of Minorities in Clinical Trials

Faster Together, Enhancing the Recruitment of Minorities in Clinical Trials Training on Coursera is designed to provide learners with a comprehensive understanding of the significance and methodologies involved in recruiting minorities for clinical trials. This course is particularly beneficial for individuals looking to expand their knowledge and expertise in the field of clinical research and professionals aiming to address healthcare disparities effectively. 

Through Faster Together, Enhancing the Recruitment of Minorities in Clinical Trials Certification by Coursera, interactive lessons and real-world case studies, participants will gain valuable insights into the barriers, strategies, and ethical considerations associated with minority recruitment in clinical trials. By exploring topics such as cultural competence, community engagement, and effective communication, learners will develop the skills necessary to promote diversity and inclusivity in clinical research. The course offers a platform to explore innovative approaches and best practices that can contribute to improving minority representation in clinical trials, ultimately leading to more equitable healthcare outcomes for all.

Also Read: 

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3 Weeks
Beginner
Free
SAS Clinical Programming Training

Offered by

Certificate

SAS Clinical Programming Training Course

90 Hours
59,500

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Offered by

Certificate

Clinical Research for beginners

Beginner
2,799

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Offered by

Certificate

Clinical Research

1,299

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