Clinical Research Associate (CRA) Diploma - CPD Certified

Key Features

• Accredited by CPD
• Instant e-certificate
• FREE PDF + Hardcopy certificate
• Easy payment method
• Fully online, interactive course with audio voiceover
• Self-paced learning and laptop, tablet, smartphone-friendly
• Learn Anytime, Anywhere
• 24/7 Learning Assistance
• Best Value Price
• Discounts on bulk purchases

The Clinical Research Associate (CRA) Diploma – CPD Certified is an all-encompassing program designed to transform learners into qualified, competent professionals in the field of clinical research. This extensive diploma offers deep insight into the clinical research industry, combining theory with real-world application across 27 CPD-certified courses. This program trains individuals to monitor clinical trials, ensure protocol compliance, manage ethical standards, and oversee accurate data collection in medical studies.

Whether you’re a beginner exploring the field or a healthcare professional seeking advancement, this diploma enables you to become a trusted link between the pharmaceutical industry and regulatory bodies. From clinical trial phases to medical writing, from pharmacovigilance to healthcare data governance, every aspect of clinical research is covered comprehensively.

Designed to be globally relevant and aligned with industry standards, this diploma is ideal for individuals aspiring to enter a rapidly expanding, high-demand sector. The curriculum includes 27 industry-relevant courses, providing a robust foundation in medical science, clinical protocols, anatomy, regulatory frameworks, and communication skills necessary for success as a Clinical Research Associate.

Learning Outcomes

• Understand clinical research phases and Good Clinical Practice guidelines
• Identify trial protocols, monitor compliance, and manage documentation
• Analyse clinical trial data and interpret medical terminology accurately
• Ensure ethical standards and regulatory compliance in clinical settings
• Apply pharmacological, genetic, and biochemistry knowledge in research
• Communicate effectively with stakeholders, teams, and trial participants

This Bundle Includes:

· Course 01: Clinical Research Administration Fundamentals

· Course 02: Research in Adult Care

· Course 03: Medical Jargon

· Course 04: Health Economics and Health Technology

· Course 05: GP – Clinical Governance

· Course 06: Clinical Coding

· Course 07: Medical Receptionist

· Course 08: Medical Law

· Course 09: Medical Transcription: Audio Typist

· Course 10: Medical Writing

· Course 11: Medical Secretary

· Course 12: Anatomy and Physiology

· Course 13: Biochemistry

· Course 14: Genetics

· Course 15: Neurology

· Course 16: Pharmacology

· Course 17: Pharmacy Assistant Diploma Level 5

· Course 18: Mental Health & Psychiatry

· Course 19: Infection Prevention, Infection Control, Infection Awareness and Infection Spread Reduction

· Course 20: Healthcare GDPR

· Course 21: Nurse Prescribing Diploma

· Course 22: Radiography

· Course 23: Handling Information in a Care Setting

· Course 24: Effective Communication Techniques for Teachers and Trainers

· Course 25: Public Health

· Course 26: Initial Training of Community Health Agents

· Course 27: Risk Management in Health & Social Care

Clinical Research Associate Bundle Description:

Course 01: Clinical Research Administration Fundamentals

Learn the foundations of clinical research management, including trial setup, monitoring, and administration. Understand roles, responsibilities, and workflow in clinical trials.

Course 02: Research in Adult Care

Explore clinical research methodologies focused on adult patient populations, ethical considerations, and trial design relevant to adult care.

Course 03: Medical Jargon

Master essential medical terminology to communicate accurately within clinical research and healthcare settings.

Course 04: Health Economics and Health Technology

Study the impact of economic factors and emerging technologies on healthcare and clinical research decision-making.

Course 05: GP – Clinical Governance

Understand governance frameworks that ensure quality and safety in general practice and clinical research environments.

Course 06: Clinical Coding

Learn standardized clinical coding systems used for accurate documentation and data management in research.

Course 07: Medical Receptionist

Develop administrative and communication skills critical for managing patient and trial participant interactions effectively.

Course 08: Medical Law

Gain insights into the legal frameworks that govern clinical research, patient rights, and compliance obligations.

Course 09: Medical Transcription: Audio Typist

Acquire skills to transcribe medical audio accurately, supporting clinical documentation and research records.

Course 10: Medical Writing

Learn how to prepare clear, precise, and compliant documents including clinical study reports, protocols, and publications.

Course 11: Medical Secretary

Understand the role of medical secretaries in organizing clinical research activities and supporting healthcare teams.

Course 12: Anatomy and Physiology

Build foundational knowledge of human body systems critical for understanding disease and treatment impacts in trials.

Course 13: Biochemistry

Explore biochemical processes and their relevance to drug development and clinical research.

Course 14: Genetics

Understand genetic principles and their application in personalized medicine and clinical trials.

Course 15: Neurology

Study neurological disorders and research approaches related to the nervous system and brain function.

Course 16: Pharmacology

Gain in-depth knowledge of drug actions, interactions, and safety assessments within clinical research.

Course 17: Pharmacy Assistant Diploma Level 5

Learn pharmaceutical operations, assisting in medication management and clinical trial drug administration.

Course 18: Mental Health & Psychiatry

Explore mental health disorders and psychiatric research methodologies relevant to clinical trials.

Course 19: Infection Prevention, Infection Control, Infection Awareness and Infection Spread Reduction

Understand infection control protocols essential to maintaining safe clinical trial environments.

Course 20: Healthcare GDPR

Learn about data protection laws and patient confidentiality in clinical research data management.

Course 21: Nurse Prescribing Diploma

Gain knowledge of nurse prescribing roles and responsibilities, linking clinical care with research protocols.

Course 22: Radiography

Study imaging techniques and their application in diagnosis and clinical research monitoring.

Course 23: Handling Information in a Care Setting

Develop skills to manage healthcare data securely and efficiently within clinical research frameworks.

Course 24: Effective Communication Techniques for Teachers and Trainers

Enhance communication skills necessary for training clinical staff and educating research teams.

Course 25: Public Health

Understand public health principles and their integration into clinical research for population-level impact.

Course 26: Initial Training of Community Health Agents

Learn community health strategies that support clinical research outreach and patient engagement.

Course 27: Risk Management in Health & Social Care

Master identifying and mitigating risks in clinical research to ensure participant safety and trial integrity.

Disclaimer:

This is an online course with pre-recorded lessons. You will get access to the course within 48 hours after your enrolment.