Advanced Monitoring In Clinical Trials

COURSE DETAILS

13 - 15 October 2014, Singapore 9.00am - 5.00pm (Reg. from 8.30am)
Singapore

Normal Course Fee: $2699
Early Bird Special: $2399 (Before 12 August 2014)
Group (>3): $2264

 

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An interactive and comprehensive course that encompasses all the aspects of clinical trials monitoring, from regulatory requirements to monitoring oversight, for all phases of a clinical trial study.

This course covers advanced and complex topics of clinical trials monitoring, and prepares experienced monitors to further expand their skills and knowledge to function at a more senior level.

 

THE PROGRAM

This course covers the advanced aspects of site management, monitoring skills and monitoring oversight. This is an interactive and comprehensive course that encompasses advanced techniques and principles in clinical trials monitoring, with reference to regulatory requirement for all phases of a clinical trial study.

The course will cover topics in sites selection, improvement in subject recruitment and retention, and issues relating to informed consent, source data verification, deviations, electronic data management, documents management, as well as communication skills in dealing with pharmacists, laboratories and ethics committee.

Note:This program is designed for professionals with at least two years of experience in the clinical research industry.

 

COURSE OBJECTIVE

  • Understand current thinking on risk based monitoring approaches and develop appropriate monitoring strategies for your study
  • Develop superior strategies for selecting sites, recruiting patients and motivating investigational sites
  • Significantly improve your performance as a monitor to an advanced level
  • Use effective planning and tracking tools to maximise efficiency as a monitor
  • Develop strategies for dealing with complex monitoring issues
  • Gain expertise in monitoring oversight activities

 

WHO SHOULD JOIN

  • Clinical Research professionals and associates
  • Clinical Scientist / Basic Scientist
  • Clinical Investigators / Principal Investigators
  • Experienced Clinical Quality Assurance Professionals
  • Project Managers
  • Clinical Study Coordinators
  • GCP-focused Regulatory Affairs Professionals
  • Professionals that had undergone basic monitoring training

 

Distinguished Trainers

Trish Parry
BSC (HONS), MRQA, CSCI

Trish Parry is an independent training and clinical research consultant with 30 years of experience in the pharmaceutical industry and 23 years of experience in clinical research. 

Trish has extensive experience in global monitoring and International clinical project management as a result of working in multi-national pharmaceutical companies including Genzyme, US Bioscience and Allergan and clinical research organisations including Quintiles.  She has set up and maintained the European Clinical Quality and Training Department in Allergan and she is an experienced trainer in clinical research and GCP. 

Trish is author of Statistics in Clinical Research (The Institute of Clinical Research, 2004) and was on the Editorial Board of the Institute of Clinical Research’s Journal, CRFocus from 2005-2014.  Trish is one of the founders of the Institute of Clinical Research Trainers Forum. 

She is a Chartered Scientist and member of Research Quality Assurance (RQA).