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Principal Investigator

Panthera BiopartnersUnited Kingdom🇬🇧United KingdomPosted 5 Aug 2026

Why This Role Stands Out

This remote Principal Investigator role offers you the chance to lead groundbreaking clinical trials in high-demand therapeutic areas, significantly impacting patient care and advancing medical research. If you are a GMC-registered specialist with a passion for clinical trials and a desire for flexible work, this opportunity to shape the future of healthcare is perfect for you. Apply today to join a patient-centric organization dedicated to excellence.

Quick Overview

Work Type
Remote
Level
Leader

Job Description

Consultant - Specialist Principal Investigators


Panthera Biopartners conduct late phase clinical trials on behalf of pharmaceutical and biotech companies in 7 Dedicated Clinical Research Sites in the UK; Preston, Rochdale, Glasgow, Enfield, York, Sheffield and Keele.


At Panthera Biopartners, we put the patient at the heart of everything we do, to ensure the best experience and environment for volunteers, participants, and employees. Due to popular demand, we are looking at expanding our Therapeutic Area offering in;


Rheumatology / Alzheimer’s / Respiratory / Neurology / Dermatology / Gastroenterology


We are in search of Consultants who would like to act as Principal Investigator for our trials in a flexible manner (combination of remote and on-site).


Role and Responsibilities:


  • Act as Principal Investigator for respective studies.
  • Provide medical oversight on clinical trial conduct at allocated site.
  • Performs PI oversight on a regular basis and available for meetings with key stakeholders.
  • Oversees staff training for the study and makes sure they are delegated on logs.
  • Holds regular meetings with the CRA and acts on any feedback given regarding site performance.
  • Participates in any internal or external audits and regulatory inspection.
  • Refer participants for respective clinical trials where appropriate.
  • Provide support to in-house sub-investigators on clinical matters when required.


Skills and Qualifications:


  • Registered as a Specialist on GMC Register (Essential)
  • GCP trained (Desirable)
  • Previous Clinical trial experience as a Sub Investigator or Principal investigator. (Desirable)


For further information please contact

Skills

GCP
Clinical Research
Clinical Trials

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