Locum Research Physician

Panthera Bio; Glasgow; On-site; GBP 90,000 - 110,000; Part time

Job summary

Panthera Biopartners seeks a Research Physician to lead site activities at our Glasgow Clinical Research Site on a locum basis, working 3 days per week (Wednesday to Friday).

The role entails ensuring adherence to protocols and SOPs, managing SAEs, coordinating staff training, and overseeing study documentation and audits under ICH/GCP guidelines. You will participate in audits and regulatory inspections and maintain up-to-date training portfolios.

Qualifications

• GMC-registered physician with license to practice in the UK.
• At least 5 years’ clinical experience with NHS experience.
• At least 1 year as Sub-Investigator on clinical trials.
• GCP training and competency.

Responsibilities

• Ensure training meets SOP/COPs and ICH/GCP, and local regulations.
• Recruit eligible patients and conduct trials per protocol.
• Maintain delegation logs and perform PI oversight weekly.
• Report Serious Adverse Events within required timeframes.
• Oversee study documentation, audits, and regulatory inspections.

Skills

GMC-registered physician

NHS clinical experience

Sub-Investigator

GCP trained

Job description

An exciting opportunity has arisen for a Research Physician to join our team at our Glasgow Clinical Research Site on a locum contract - 3 X Days Per Week (Wednesday to Friday)

Role and Responsibilities

• As Principal investigator you will need to ensure all training is met for each member of the research site, not only for the specific study but making sure all SOP/COPs are adhered to and ICH/GCP and any local regulations are met.
• Ensuring all clinical trials are conducted according to Protocol, recruiting patients who are eligible for the study.
• Adhere to the study delegation logs as to specific tasks to be performed by you.
• Whenever Serious Adverse Events/Adverse Events occur, these are reported on within the time scale outlined.
• Look after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.
• All study documentation should be legible, concise and accurate. This should be signed off and any queries dealt with within the agreed timeframes.
• Work within the guidelines of the company SOP/COPs.
• Participation in the out of hours/on call rota which is set out for all Panthera Research Physicians is mandatory.
• Working at other Panthera sites or working different hours or days will be required on occasion.
• Competency assessments should be performed every 3 months. A training portfolio should always be kept up to date. Any training should be signed of in a timely manner.
• Has overall responsibility of the study at site
• Performs PI oversight on a regular basis at least once a week.
• Oversees staff training for the study and makes sure they are delegated on logs.
• Ensures the quality of all study documentation.
• 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.

Mandatory skills and Qualifications:

• GMC registered physician with license to practice in the UK.
• At least 5 years’ clinical experience with at least 1 year in the NHS.
• At Least 1 Year as Sub - Investigator
• GCP Trained

Panthera Biopartners is an equal opportunity employer. Panthera will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. Panthera only employs individuals with the right to work in the country where the role is advertised.

AI - Please note, AI may be used in our recruitment process however all CV's are manually viewed by the team.

Panthera Biopartners

Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience.

We put the patient at the heart of everything we do, to ensure the best experience and environment for volunteers, participants, and employees. We want people who are swift to action, confident to lead, willing to collaborate and curious about what science can do.