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Clinical Trial Administrator (CTA) premium bundle consists of 30 precisely chosen courses on a wide range of topics essential for anyone looking to excel in this field. Each segment of Clinical Trial Administrator (CTA) is meticulously designed to maximise learning and engagement, blending interactive content and audio-visual modules for a truly immersive experience. Certification You have to complete the assignment given at the end of the Clinical Trial Administrator (CTA) course. After passing the Clinical Trial Administrator (CTA) exam You will be entitled to claim a PDF & Hardcopy certificate accredited by CPD Quality standards completely free. CPD 300 CPD hours / points Accredited by CPD Quality Standards Who is this course for? This Clinical Trial Administrator (CTA) course is ideal for: Students seeking mastery in Clinical Trial Administrator (CTA) Professionals seeking to enhance Clinical Trial Administrator (CTA) skills Individuals looking for a Clinical Trial Administrator (CTA)-related career. Anyone passionate about Clinical Trial Administrator (CTA) Requirements This Clinical Trial Administrator (CTA) doesn't require prior experience and is suitable for diverse learners. Career path Clinical Trial Manager Clinical Research Coordinator Clinical Operations Manager Clinical Project Manager Director of Clinical Operations Certificates CPD Accredited Digital certificate Digital certificate - Included CPD Accredited Hard copy certificate Hard copy certificate - Included If you are an international student, you will be required to pay an additional fee of 10 GBP for international delivery, and 4.99 GBP for delivery within the UK, for each certificate
Overview Explore the intricacies of clinical research and understand the administration process with our Clinical Research Administration Training course. This course will help you deepen your knowledge and acquire the ability to seek career prospects in the relevant sectors. The course is packed with high;y valuable information on clinical research. From the informative modules, you will learn the core concepts of clinic trial designing and planning. The course will help you develop the skills for data management and analysis. You will be able to build your expertise in monitoring and auditing. Moreover, you will acquire the skills required for quality control and site management as well. After the course, you will receive a CPDQS-accredated certificate of achievement. This certificate will enhance your employability and help you reach your career goals. Enrol now! Course Preview Learning Outcomes Understand the significance of clinical research in healthcare Learn about the process of clinical trail design and planning Deepen your knowledge of ethics and regulatory compliance Develop the ability for data management and record-keeping Know how to monitor and audit the trials Grasp the process of study site management and quality control Why Take This Course From John Academy? Affordable, well-structured and high-quality e-learning study materials Engaging tutorial videos, materials from the industry-leading experts Opportunity to study in a user-friendly, advanced online learning platform Efficient exam systems for the assessment and instant result Earn UK & internationally recognised accredited qualification Easily access the course content on mobile, tablet, or desktop from anywhere, anytime Excellent career advancement opportunities Get 24/7 student support via email. What Skills Will You Learn from This Course? Trail planning Data management and analysis Monitoring and auditing Site management Quality control Compliance management Who Should Take This Clinical Research Administration Training? Whether you're an existing practitioner or an aspiring professional, this course is an ideal training opportunity. It will elevate your expertise and boost your CV with key skills and a recognised qualification attesting to your knowledge. Are There Any Entry Requirements? This Clinical Research Administration Training course is available to all learners of all academic backgrounds. But learners should be aged 16 or over to undertake the qualification. And a good understanding of the English language, numeracy, and ICT will be helpful. Certificate of Achievement After completing this course successfully, you will be able to obtain an Accredited Certificate of Achievement. Certificates & Transcripts can be obtained either in Hardcopy at £14.99 or in PDF format at £11.99. Career Pathâ This exclusive Clinical Research Administration Training course will equip you with effective skills and abilities and help you explore career paths such as Clinical Research Administrator Clinical Research Associate Clinical Research Coordinator Clinical Data Manager Module 01: Introduction to Clinical Research Administration Introduction to Clinical Research Administration 00:15:00 Module 02: Clinical Trial Design and Planning Clinical Trial Design and Planning 00:11:00 Module 03: Ethics and Regulatory Compliance Ethics and Regulatory Compliance 00:13:00 Module 04: Institutional Review Boards (IRBs) and Ethics Committees Institutional Review Boards (IRBs) and Ethics Committees 00:10:00 Module 05: Data Management and Recordkeeping Data Management and Recordkeeping 00:12:00 Module 06: Safety Reporting and Adverse Events Safety Reporting and Adverse Events 00:10:00 Module 07: Clinical Trial Monitoring and Auditing Clinical Trial Monitoring and Auditing 00:09:00 Module 08: Study Site Management and Quality Control Study Site Management and Quality Control 00:17:00 Module 09: Data Analysis and Reporting Data Analysis and Reporting 00:09:00 Module 10: The Future of Clinical Research The Future of Clinical Research 00:10:00 Certificate and Transcript Order Your Certificates and Transcripts 00:00:00
Good Clinical Practice (GCP) is a set of internationally recognised ethical and scientific quality requirements for designing, conducting, recording and reporting clinical trials. Compliance with GCP principles is required by regulatory authorities in many countries for the authorisation of clinical trials and the acceptance of their data. The International Council for Harmonisation’s guideline E6, often referred to as ICH GCP, is the international standard specification for Good Clinical Practice.
A clinical investigator is responsible for conducting the clinical trial in compliance with the study protocol, GCP, medical ethics, and applicable legal requirements. The clinical research community expects that investigators and clinical staff are fully trained in GCP. Duties and functions discussed in this short course include: provision of adequate resources; liaison with IRB/IEC; compliance with protocol; management of investigational product(s), informed consent and data records; and safety reporting.