Medical Consultant

Panthera Biopartners; United Kingdom; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

Panthera Biopartners seeks a Consultant to act as Principal Investigator for late-phase trials across Rheumatology, Alzheimer’s, Respiratory, Neurology, Dermatology and Gastroenterology in the UK, with a flexible mix of remote and on-site work.

The role requires GMC Specialist registration with prior clinical trial experience as PI or sub-investigator, and candidates should be prepared to oversee site staff and participate in audits.

Qualifications

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

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

GCP trained

Clinical trial experience as PI/Sub-In

Education

GMC Specialist registration

Job description

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)