Principal Investigator Training Programme
About
The Principal Investigator Training Programme (PITP), sponsored by the ICC-CTN and recognised by the Joint Faculty of Intensive Care Medicine of Ireland (JFICMI), is a formalised system for non-consultant hospital doctors (NCHDs) to train in the delivery of large clinical trials.
The PITP is a six-month training opportunity that provides practical research experience for NCHDs interested in starting a research career and can be undertaken in parallel with clinical training without significant additional commitment. During the six months, the candidate selects a multicentre clinical trial of interest and is linked with the principal investigator for that trial at their hospital. The candidate becomes an essential member of the clinical research team for that trial and completes a logbook of learning activities that are verified by the principal investigator. On successful completion, a certificate is issued that formally recognises the candidate’s contribution, and the ICC-CTN will recommend to the trial leadership that the candidate is acknowledged in any publications resulting from their work. The candidate will also gain access to a wide variety of educational materials and an online lecture series delivered by the PITP.
The certification process is primarily delivered through the online logbook (link).
Aims
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To formally recognise Irish NCHDs’ contribution to multicentre clinical research
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To embed optional participation in clinical research within medical training
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To add trainees to the current research infrastructure throughout Ireland by creating a research-positive atmosphere and teaching practical delivery of multicentre studies
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To create a network of alumni who go on to lead clinical research of their own or act as local advocates for the delivery of multicentre studies
Curriculum / Schedule of Activities
Log
Maintenance of study delegation log
Screening
Screening of potential participants
Eligibility
Confirmation of participant eligibility
Consent
Consent
SAE Monitoring
Monitoring for serious adverse events (SAEs), if applicable
SAE Reporting
Reporting serious adverse events (SAEs), if applicable
IMP Prescribing
Prescription of investigational medicinal product (IMP), if applicable
Bio Sampling
Collection and processing of biological samples, if applicable
Data Entry
Data entry
Promotion
Promotion of the study to the wider department
Meetings
Attendance at site investigator meetings
Barriers
Identification of local barriers to study recruitment, proposing ways to overcome these barriers, and feeding this back to local PI
Reflections
Additional reflections