Principal Investigator - Clinical Pharmacology

Location
Belfast (County)
Salary
Competitive
Posted
10 Jun 2021
Closes
10 Jul 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Management

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…

Pre-study Requirements:

  • 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

During and Post Study:

  • 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

Requirements:

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

Benefits:

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

Get in touch...

  • Contact: Vincenzo B. Dessena BSc. MSc.
  • Clinical Development and Medical Affairs Recruitment Consultant
  • Email: vdessena (at) barringtonjames.com

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