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Overview
Trials that are successfully delivered on time and to the recruitment target require the employment of good project management. High quality data is driven through data and quality management processes, and these must be combined with an understanding of the trial safety reporting requirements, and the ongoing assessment and evaluation of trial risks.
Key facts
The Clinical Trial Management - Maximising Effectiveness (Online) programme at the University of Birmingham will explore how to plan for and respond to clinical trial challenges, maximising effectiveness, efficiency and data quality. It is aimed at individuals involved in trial co-ordination and management who have some experience, and who would like to build on this skill set.
Programme Structure
Learning outcomes:- Determine the factors that may contribute to the success or failure of a trial project plan for site and participant recruitment.
- Defend the implementation of flexible and adaptive trial management plans.
- Analyse the impact of one amendment or change on wider aspects of the trial.
- Describe the key risks to trial data, and formulate strategies and tools to maximise data quality.
- Discuss the potential challenges in the management of trial safety data, and propose solutions for effective trial management.
- Identify the potential barriers to effective communication, and analyse the impact of these barriers on efficient trial delivery.
Key information
Duration
- Part-time
- 2 days
Start dates & application deadlines
- StartingApplication deadline not specified.
- StartingApplication deadline not specified.
Language
English
Delivered
Online
Campus Location
- Birmingham, United Kingdom
Disciplines
Health Sciences View 283 other Short Courses in Health Sciences in United KingdomWhat students do after studying
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Academic requirements
We are not aware of any specific GRE, GMAT or GPA grading score requirements for this programme.
English requirements
We are not aware of any English requirements for this programme.
Other requirements
General requirements
- This course is suitable for individuals working within academic CTUs, NHS Trusts or industry who on behalf of the sponsor manage the trial and/or the data.
- This includes Trial Co-ordinators, Trial Managers, Data Managers, Project Managers, Trial Administrators & Research Nurses.
- The focus is on managing the trial from the sponsor perspective.
Tuition Fees
Tuition fees are shown in and the most likely applicable fee is shown based on your nationality.
-
International Applies to you
Applies to youNon-residents250 GBP / full≈ 250 GBP / full -
Domestic Applies to you
Applies to youCitizens or residents250 GBP / full≈ 250 GBP / full
Funding
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