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Biometrics in Clinical Trials

Biometrics in Clinical Trials

Date to be announced

Contact us for more info
Price available after dates are announced

TRAINING TIMES

  • TBDVienna
  • TBDLondon
  • TBDNew York
  • TBDLos Angeles
Online Training

WHY SHOULD YOU ATTEND?

Get a structured overview of Biometrics in Clinical Trials

Get a practical overview from Study Protocol to Study Report

Data management, statistical programming and eClinical systems

Functions and importance of data management and biostatistics in clinical trials.

Navigate Key Regulatory Frameworks

Gain insights into ICH E6 and E3 guidelines, GDPR, and the EU Clinical Trials Regulation applied to clinical studies.

Discover Statistical Outputs and Reporting

Understand the creation and purpose of TLFs and the structure and statistical basis of the clinical study report.


OUR ONLINE TRAINING EXPERIENCE INCLUDE

Two days of expert-led Zoom sessions packed with discussions, Q&As, and real-world scenarios.

All slides, tools, and supporting materials available in our CLIENT ZONE before, during, and after the course.

Receive a digital certificate (also Linkedin-ready) that verifies your skills in strategic trial planning.


LEARNING OBJECTIVES

Learning Objective

Understand the Role of Biometrics

Learn about the functions of data management, statistical programming, and biostatistics in clinical trials.

Learning Objective

Navigate Key Regulatory Frameworks

Gain insights into ICH E6 and E3, GDPR, and the EU Clinical Trials Regulation, GAMP5 and their applications.

Learning Objective

Explore the Study Lifecycle

Understand the end-to-end process from study protocol development to the clinical study report.

Learning Objective

Learn Data Collection and Standards

Understand what data is collected, stored and the role of CDISC standards (CDASH, SDTM, ADaM).

Learning Objective

Discover Statistical Outputs and Reporting

Understand the creation and purpose of TLFs and the structure and statistical basis of the clinical study report.

Learning Objective

Build Practical Understanding

Apply real-world examples and group discussions to strengthen understanding of biometrics processes.


WHO IS THIS TRAINING FOR?

Designed for professionals who want to enhance their expertise and advance their careers

Clinical Trial Managers

Data Managers

Statistical Programmers

Biostatisticians

Project Managers

Regulatory Affairs Specialists

Clinical Data Managers

Biometric systems specialists


KEY TOPICS

Biometrics History and Regulatory Foundations
Clinical Study Report (CSR) Structure
ICH E6 and Data Integrity
CDISC Standards in Biometrics
Biostatistics and Statistical Programming
Clinical Data Management Processes
Types of data and Best Practices in Reporting
Overview of eClinical Systems
FDA and EMA Guidelines
Early phase: Pharmacokinetics (PK)

TRAINER

Simone Ahrens-Mende

Simone Ahrens-Mende

Biometrics Specialist, Ahrens-Mende Associates

Simone Ahrens-Mende holds a Diploma in Mathematics and a Master’s degree in Clinical Trial Management. She is a highly experienced leader in clinical research, with over 25 years of expertise in Data Management, Statistical Programming, and Biostatistics. Throughout her career, she has held senior positions in international CROs, where she has successfully led cross-functional teams, optimized clinical processes, and ensured compliance with global regulatory standards. Simone is known for her strategic leadership, process innovation, and dedication to quality, having contributed to the success of numerous clinical trials across various therapeutic areas. She brings a unique combination of technical expertise and a strong commitment to mentoring and developing professionals in biometrics and clinical research. We are live on webchat!

Learn More →

Video Invitation

Watch the video invitation from the trainer.

Sneak peek

Sneak Peek

Take a sneak peek at the trainer's presentation.

View PDF →