This advanced course comprehensively explores clinical trial methodology, focusing on clinical trials' design, conduct, and analysis. Participants will gain an in-depth understanding of the principles and practices essential for conducting high-quality clinical research. The course combines theoretical instruction with practical applications, preparing healthcare professionals and researchers to effectively design and manage clinical trials.

Upon completion of this course, participants will be able to:

Understand the fundamental principles of clinical trial design.
Develop skills in conducting and managing clinical trials.
Learn advanced methods for analysing clinical trial data.
Gain knowledge of regulatory and ethical considerations in clinical research.
Enhance their ability to communicate clinical trial results effectively.

This course is intended for:

Clinical researchers
Medical practitioners
Healthcare professionals involved in clinical trials
Data analysts in health sciences
Regulatory affairs specialists
Graduate students in clinical research and related fields

The course employs a blend of instructional methods, including:

Interactive lectures
Hands-on trial design and analysis sessions
Group discussions and case studies
Expert-led Q&A sessions
Comprehensive course materials and resources

Day 5 of each course is reserved for a Q&A session, which may occur off-site. For 10-day courses, this also applies to day 10

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ID	التواريخ المتاحة	المدينة	الرسوم	الإجراءات

Course Content

Section 1: Introduction to Clinical Trials

Overview of clinical trial phases and types
Key concepts in clinical trial design
Ethical considerations and informed consent

Section 2: Designing Clinical Trials

Formulating research questions and hypotheses
Randomisation methods and control groups
Sample size calculation and power analysis

Section 3: Conducting Clinical Trials

Recruitment and retention of study participants
Data collection methods and management
Monitoring and ensuring trial quality

Section 4: Analyzing Clinical Trial Data

Statistical methods for clinical trial analysis
Handling missing data and protocol deviations
Interpreting and reporting trial results

Section 5: Practical Applications and Case Studies

Developing a clinical trial protocol
Case studies and collaborative problem-solving
Communicating findings to stakeholders
Course review and expert Q&A

Certificate Details

عند إتمام هذه الدورة التدريبية بنجاح، سيحصل المشاركون على شهادة إتمام التدريب من Holistique Training. وبالنسبة للذين يحضرون ويكملون الدورة التدريبية عبر الإنترنت، سيتم تزويدهم بشهادة إلكترونية (e-Certificate) من Holistique Training.

شهادات Holistique Training معتمدة من المجلس البريطاني للتقييم (BAC) وخدمة اعتماد التطوير المهني المستمر (CPD)، كما أنها معتمدة وفق معايير ISO 9001 وISO 21001 وISO 29993.

يتم منح نقاط التطوير المهني المستمر (CPD) لهذه الدورة من خلال شهاداتنا، وستظهر هذه النقاط على شهادة إتمام التدريب من Holistique Training. ووفقًا لمعايير خدمة اعتماد CPD، يتم منح نقطة CPD واحدة عن كل ساعة حضور في الدورة. ويمكن المطالبة بحد أقصى قدره 50 نقطة CPD لأي دورة واحدة نقدمها حاليًا.