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Online Master’s Degree in Introduction to Clinical Research

Price

GBP 1100

Duration

12 Months

Online Master’s Degree in Introduction to Clinical Research

Course Overview:

The Master’s Degree in Introduction to Clinical Research is designed to provide medical and healthcare professionals with a solid foundation in clinical research methodologies, data analysis, and ethical considerations. This program offers a comprehensive understanding of clinical trials, research design, and data interpretation, equipping graduates with the skills needed to conduct and manage clinical research effectively. The course is delivered entirely online, offering flexibility for professionals worldwide.

Key Features:

  • 100% Online Delivery: Flexible learning options allow students to study from anywhere in the world.

  • In-Depth Curriculum: Covers clinical research design, data management, statistical analysis, and research ethics.

  • Interactive Learning: Features multimedia content, virtual simulations, and case-based learning.

  • Accreditation: Accredited by relevant medical and educational bodies.

  • Free Certificate Delivery: Certificates are delivered globally at no extra cost; e-certificates are immediately available upon completion.

  • No Mention of Online Study on Certificate: The certificate you receive will not indicate that the course was conducted online.

  • International Enrollment: Open to medical professionals globally.

  • International Recognition: Allows foreign doctors to work in the UK without the need to pass the PLAB exams.

Technical Hours:

  • Total Study Hours: Estimated at approximately 1,200 hours.

    • Theory: 900 hours

    • Practical Work: 300 hours

Duration and Structure:

  • Program Duration: 12 months

  • Delivery Mode: Entirely online

  • ECTS Credits: 60

Price:

  • Full Fee: GBP 1100 One Time Full Payment 

Eligibility:

  • Educational Qualification: Requires a medical degree (MBBS or equivalent).

  • Professional Experience: Experience in clinical research or related fields is preferred but not mandatory.

  • International Candidates: The course is open to applicants globally.

General Objectives:

  • Understand Research Design: Develop a comprehensive understanding of clinical research design and methodology.

  • Conduct Data Analysis: Gain proficiency in data management and statistical analysis relevant to clinical research.

  • Apply Research Ethics: Learn to navigate the ethical considerations and regulatory requirements in clinical research.

  • Manage Clinical Trials: Acquire skills in managing and monitoring clinical trials, including participant recruitment and data collection.

  • Implement Evidence-Based Practices: Apply evidence-based practices to improve research outcomes and contribute to the advancement of medical knowledge.

Course Modules:

  1. Introduction to Clinical Research

    • Description: Overview of clinical research, including key concepts, study designs, and the role of clinical research in healthcare.

    • Skills: Understanding of basic research principles and study designs.

    • Key Features: Interactive lectures, foundational readings.

    • Teaching Hours: 80 hours

  2. Clinical Research Methodologies

    • Description: Detailed examination of various research methodologies, including randomized controlled trials, cohort studies, and case-control studies.

    • Skills: Ability to design and implement different research methodologies.

    • Key Features: Virtual simulations, research design exercises.

    • Teaching Hours: 120 hours

  3. Statistical Analysis in Clinical Research

    • Description: Introduction to statistical methods and software used in clinical research.

    • Skills: Proficiency in statistical analysis, interpretation of research data.

    • Key Features: Hands-on tutorials with statistical software, data analysis exercises.

    • Teaching Hours: 120 hours

  4. Ethics and Regulatory Compliance

    • Description: Exploration of ethical issues, regulatory requirements, and best practices in clinical research.

    • Skills: Understanding of research ethics, regulatory compliance, and patient consent.

    • Key Features: Case studies, interactive modules on ethical dilemmas.

    • Teaching Hours: 100 hours

  5. Clinical Trial Management

    • Description: Skills and knowledge necessary for managing and monitoring clinical trials, including participant recruitment and data management.

    • Skills: Proficiency in trial management, data monitoring, and compliance.

    • Key Features: Virtual trial management scenarios, management tools.

    • Teaching Hours: 120 hours

  6. Data Management and Quality Control

    • Description: Techniques for managing research data, ensuring data quality, and implementing quality control measures.

    • Skills: Data management, quality assurance, and control techniques.

    • Key Features: Interactive data management exercises, quality control workshops.

    • Teaching Hours: 100 hours

  7. Research Proposal Development

    • Description: Development of research proposals, including problem identification, literature review, and proposal writing.

    • Skills: Ability to create and present research proposals.

    • Key Features: Proposal writing workshops, peer reviews.

    • Teaching Hours: 90 hours

  8. Capstone Project

    • Description: An independent research project where students apply their knowledge to a real-world research question or issue.

    • Skills: Project management, research execution, and presentation.

    • Key Features: Personalized mentorship, project presentations.

    • Teaching Hours: 150 hours

Learning Outcomes:

Upon completion of this program, students will:

  • Research Design Expertise: Demonstrate a thorough understanding of clinical research design and methodologies.

  • Data Analysis Skills: Apply statistical methods and software to analyze and interpret clinical research data.

  • Ethical Compliance: Navigate ethical considerations and regulatory requirements in clinical research.

  • Trial Management: Effectively manage and monitor clinical trials, ensuring data integrity and compliance.

  • Evidence-Based Practices: Implement evidence-based practices to enhance research outcomes and contribute to medical knowledge.

  • Project Management: Develop and present research proposals and complete an independent research project.

How to Join the Academy:

  • Start Studying Immediately: No registration required; gain instant access.

  • Instant Access: Receive your username and password immediately after payment.

Enrollment Steps:

  1. Complete Enrollment: After payment, receive your username and password. Log in to upload your MBBS degree and enter your name as per your passport.  if the degree is found to be fake, your course will be canceled, and a refund will be processed within 5 days.

  2. Start Your Studies: Access all course materials, interactive modules, and assignments via our online platform.

  3. Complete the Program: Engage with the content, participate in discussions, and complete assignments.

  4. Obtain Certification: Receive your Master’s Degree in Introduction to Clinical Research. The certificate will be delivered to your residence free of charge, including international delivery. You can also download an e-certificate directly from your course page upon completion.

Refund Policy:

  • 30-Day Refund Policy: To request a refund:

    • Log In to Your Account: Use your credentials to access your account.

    • Navigate to Your Course Page: Locate your enrolled course.

    • Request Cancellation: Initiate the cancellation process directly from your course page.

    • Refund Processing: We will process your full refund within 5 days of cancellation.

NHS-UK -GMC UK

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