GMC Registered Doctor

Panthera Bio; United Kingdom; Hybride; GBP 90 000 - 120 000; Plein temps

Résumé du poste

Panthera Biopartners invites consultants to act as Principal Investigator for late-phase trials across multiple therapeutic areas, combining remote and on-site responsibilities in the UK.

Responsibilities include medical oversight, staff training, regular CRA liaison, and participation in audits and regulatory inspections to ensure trial integrity and patient safety.

Qualifications

• Registered as a GMC Specialist (Essential).
• GCP training (Desirable).
• Experience as PI or Sub-Investigator in clinical trials (Desirable).

Responsabilités

• 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 is available for meetings with key stakeholders.
• Oversees staff training and ensures delegation on logs.
• Holds regular meetings with the CRA and acts on feedback regarding site performance.
• Participates in audits and regulatory inspections.
• Refer participants for respective trials where appropriate.
• Provide support to in-house sub-investigators on clinical matters when required.

Connaissances

GMC Specialist

GCP trained

Clinical trial PI/Sub-Investigator

Description du poste

Consultant - Rheumatology / Alzheimer's / Respiratory / Neurology / Dermatology / Gastroenterology

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 [e-mail]