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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

  • To formally recognise Irish NCHDs’ contribution to multicentre clinical research

  • To embed optional participation in clinical research within medical training

  • To add trainees to the current research infrastructure throughout Ireland by creating a research-positive atmosphere and teaching practical delivery of multicentre studies

  • 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