ACDM Level One Accredited Training Program


Level One Accredited Training Program
Clinical Data Management – Fundamental Skills

Face-To-Face Training Session (2 Days): 16th - 17th March 2015 (venue TBC)

Course Overview – why should you attend?

Regulators are increasingly requesting evidence of competence. Experience alone does not provide evidence of competence. The ACDM, in partnership with the International Academy of Clinical Research, has developed a series of training programs supported by comprehensive course work and interactive sessions, providing independently recognized, competence-based accreditation to support the continued professional development of staff involved in the management of clinical trial data.

Continuing Professional Development (CPD) is a way for professionals to demonstrate that they continue to learn and develop throughout their careers, to keep their skills and knowledge up to date and are able to work competently.

CPD points are related to the notional learning hours in taking a course and include any learning hours spent on pre-course work and any post-course work. The latter includes collecting the learning evidence on the job and taking part in the assessment process.

Each of the ACDM’s courses has been assigned a number of CPD points based on the time involved in participating in the course and in completing assigned pre- and post-course work.
The courses are quality assured by bodies regulated by Ofqual (Office for Qualifications and Examinations Regulation) and the levels are recognized within the ISCED framework (International Standard of Education) framework produced by UNESCO (United Nations Educational, Scientific and Cultural Organization).

The Level One Accredited Training Program in Clinical Data Management is aimed at developing essential core clinical data management skills. The training courses are highly interactive and supported by comprehensive materials and evaluated course work.

Who should attend?

This course is aimed at data management professionals who have some hands-on experience across data management or are new to the data management role.

Course learning objectives

  • Understand the clinical trial process
    • Explain the clinical trial process including the purpose of the clinical trial protocol, statistical analysis plan and clinical study report
    • Describe the typical study team roles and responsibilities in a clinical trial
  • Understand the role of the data management function within the clinical trial process
    • Describe the purpose of the Data Management Plan
    • Explain the aims of data validation
    • Describe different types of database lock and their appropriate use
  • Know how clinical research is regulated
    • Explain the key elements of the International Conference on Harmonisation of Good Clinical Practice (ICH GCP)
    • Explain the purpose of the regulatory bodies in Europe, USA and Japan
    • Explain the purpose of SOPs
  • Understand how to deliver high quality clinical data for analysis
    • Describe a suite of data validation checks for a sample study
    • Explain how a manual data query could be resolved by the responder on the first attempt
    • Explain the purpose of coding clinical data with the medical Dictionary for Regulatory Activities (MedDRA)

Course Format

This course will be deliverd as a Face-to-Face session over 2 days. Comprehensive course materials are provided and delegates will be expected to successfully complete pre and post-course work in order to complete the accredited program.

Registration Information:

Training Course Participation is £1500 plus VAT for ACDM members (£1770 plus VAT for non-members). 

Click here to book online

We look forward to seeing you at this new and exciting training course!

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