Principal Investigator – Early Phase Clinical Development

Region: Europe
Area: Ireland
Location: Unspecified
Posted: 11th May 2021

I am working with a successful clinical research facility, focused on translational research and clinical pharmacology. They pride themselves in innovative research solutions to get new drugs to market quickly and effectively, with one of the most experienced clinical pharmacology networks in the industry.

We are seeking a principal investigator/ Clinical physician to join an experienced and fast growing clinical research team. You will be using your medical expertise to assume responsibility of phase I study participant’s safety as well as the quality of the clinical trials.

If you are looking for the opportunity to support life-saving treatments, where you can combine your medical expertise with clinical studies, please read further.


  • Attending study meetings with sponsors
  • Reviewing protocol and Investigator brochures for feasibility and safety, whilst building and maintaining relationships with sponsors
  • Preparing REC submissions and reviews and constant communication with the REC during protocol approval and subject issues
  • Final review of process data, medical history and lab work prior to authorization of subjects participating in the studies
  • Managing adverse events
  • Reviewing pre-dose lab work, study data and ECG’s and create a study plan on the results
  • Safety data review with sponsor
  • Review and reporting of SAE’s to sponsor and REC within timelines
  • Safety monitoring and follow up of adverse events and psychical exams
  • Review and sign off of case studies and reports at the end of the study
  • Inform the REC of study completion
  • Assisting with identifying and maintaining a study physician network for contract operations
  • Assisting in the design and scheduling of specialist medical procedures
  • Training clinic associates on CPR and assessment skills
  • Assisting department on medical SOP’s and training plans
  • Participating in the weekly review of study results


  • MD, with active GMC registration
  • First in human accreditation or clinical pharmacology or pharmaceutical medicine training
  • Experience on phase FIH/ Phase I or Phase II clinical trials
  • Experience with regulatory elements of clinical trials


  • Highly competitive basic salary
  • Relocation package
  • Clear internal promotion pathway
  • Spearhead the development of novel therapeutics

Following your application Adam Bloomfield, a specialist Pharmaceutical Recruiter with over 3 years’ experience recruiting in the field will discuss the opportunity with you in detail. He will be more than happy to answer any questions relating to the industry and the potential for your career growth. The conversation can also progress further to discussing other opportunities, which are also available right now or will be imminently becoming available.

This position has been highly popular, and it is likely that it will close prematurely. We recommend applying as soon as possible to avoid disappointment. Please click ‘apply’ or contact Adam Bloomfield for any further information.

Adam J. Bloomfield

Principal Scientific Consultant – EMEA

Email: abloomfield (at)

About Your Consultant

I am a Senior Specialist Clinical Development, and Medical Affairs Consultant covering the European region. The pharmaceutical industry is a genuine passion of mine having attained first-class classification in both my Biomedicine BSc. and a Molecular Medicine MSc. Therefore, I maintain expert-level, credible, knowledge within the European market with insights on the lastest development programs. Thus, I strongly believe in the importance of finding the most-suitable candidates for any of my clients. My predominant focus at BarringtonJames is to apply my extensive knowledge, experience, and resources in sourcing only the most specific and best candidates for life science companies.

Email: Telephone: 01293776644

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