Medical Director

Feladatok: This is an exciting opportunity for an individual who is passionate about clinical research, physician leadership and delivering high-quality patient care and who wants to play a key role in supporting OEC's continued growth and success. The role will provide medical oversight, leadership and support to research physicians across the region with a strong focus on driving operational and clinical excellence. 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 outlinedLook after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Look after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Has overall responsibility of the study at sitePerforms PI oversight on a regular basis at least once a weekOversees staff training for the study and makes sure they are delegated on logsEnsures the quality of all study documentationHolds regular meetings with the CRA and acts on any feedback given regarding site performanceParticipates in any internal or external audits and regulatory inspectionAs 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 outlinedLook after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Look after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Has overall responsibility of the study at sitePerforms PI oversight on a regular basis at least once a weekOversees staff training for the study and makes sure they are delegated on logsEnsures the quality of all study documentationHolds regular meetings with the CRA and acts on any feedback given regarding site performanceParticipates in any internal or external audits and regulatory inspection Elvárások: This is an exciting opportunity for an individual who is passionate about clinical research, physician leadership and delivering high-quality patient care and who wants to play a key role in supporting OEC's continued growth and success. The role will provide medical oversight, leadership and support to research physicians across the region with a strong focus on driving operational and clinical excellence. 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 outlinedLook after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Look after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Has overall responsibility of the study at sitePerforms PI oversight on a regular basis at least once a weekOversees staff training for the study and makes sure they are delegated on logsEnsures the quality of all study documentationHolds regular meetings with the CRA and acts on any feedback given regarding site performanceParticipates in any internal or external audits and regulatory inspectionAs 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 outlinedLook after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Look after the wellbeing of the trial participant and make referrals for the patient to third parties or patients own GP as appropriate.Has overall responsibility of the study at sitePerforms PI oversight on a regular basis at least once a weekOversees staff training for the study and makes sure they are delegated on logsEnsures the quality of all study documentationHolds regular meetings with the CRA and acts on any feedback given regarding site performanceParticipates in any internal or external audits and regulatory inspection

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