PANTHERA SITE TOUR !

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If this sounds like you, then you’re our kind of person!
As a distinguished professional in the Healthcare & Research sector, you will be at the forefront of our growth. As we look to accelerate our clinical breakthroughs for our patients, customers, and future generations. We are looking for a forward-thinking individual with excellent communication skills. This candidate should be proactive and striving to grow and succeed with the organisation. Want to know more about Clinical Research? We have you covered on the video below.

MANDATORY SKILLS AND QUALIFICATIONS:

• GMC registered physician with license to practice in the UK.
• Medical Registrar level

DESIRED SKILLS AND REQUIREMENTS

• GCP trained.
• Previous Clinical trial experience as a Sub Investigator or Principal investigator.

• 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.