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Lead Project Manager - GI & Lymphoma | The Royal Marsden NHS Foundation Trust
The Royal Marsden NHS Foundation Trust | Sutton | findajob.dwp.gov.uk |
Lead Project Manager (Clinical Trials) -GI & Lymphoma
Our sponsored GI/Lymphoma cancer clinical research portfolio is both world-leading and
practice changing. This is a unique opportunity to help develop, oversee and deliver an
exciting portfolio and team dedicated to advancing clinical practice in GI/Lymphoma cancer.
This post is responsible for the development, oversight and delivery of the GI/Lymphoma portfolio managed within RM CTU. The post holder is expected to have at least 5 years’ experience in running multi centre complex CTIMP sponsored studies.
There are three key domains to the post - project management, team management and portfolio management: in addition to corporate contribution.
The post-holder will project manage a number of complex Medicines and Healthcare products Regulatory Agency (MHRA) regulated clinical trials, ensuring that they are set-up, delivered, and closed-down in accordance with Good Clinical Practice (GCP) and all applicable regulations.
The post therefore requires a clinical research professional with
extensive experience of sponsor-level management of clinical trials in an academic environment.
The post-holder will establish, develop and manage a growing team of senior trial managers and data managers, each of which will work on their own portfolio of sponsored studies. The post will oversee the line management of these staff and prioritise and allocation workload to
ensure effective and efficient trial management and delivery.
The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer.
We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Daycare Unit in Kingston Hospital.
At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.
At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance.
We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.
For further information on this role, please see the attached detailed Job Description and Person Specification
Liaise closely with the CI, database programmer, statistician and other key members of the clinical trial study team (i.e. clinical fellow) to ensure on-going clinical, scientific and operational oversight.
Be a point of contact for participating sites, sponsor(s), funder(s), pharmaceutical partners, regulatory authorities and the trial oversight committees.
Oversee the day-to-day conduct of the study at participating sites, providing support and advice and addressing any logistical issues as they arise.
Organise regular meetings as needed to facilitate the efficient management of the clinical trial, preparing the agenda and meeting papers, and provide minutes following the meeting in a timely manner.
Ensure timely data collection and receipt / transfer of any clinical materials or samples for clinical trials.
This advert closes on Wednesday 8 May 2024
Our sponsored GI/Lymphoma cancer clinical research portfolio is both world-leading and
practice changing. This is a unique opportunity to help develop, oversee and deliver an
exciting portfolio and team dedicated to advancing clinical practice in GI/Lymphoma cancer.
This post is responsible for the development, oversight and delivery of the GI/Lymphoma portfolio managed within RM CTU. The post holder is expected to have at least 5 years’ experience in running multi centre complex CTIMP sponsored studies.
There are three key domains to the post - project management, team management and portfolio management: in addition to corporate contribution.
The post-holder will project manage a number of complex Medicines and Healthcare products Regulatory Agency (MHRA) regulated clinical trials, ensuring that they are set-up, delivered, and closed-down in accordance with Good Clinical Practice (GCP) and all applicable regulations.
The post therefore requires a clinical research professional with
extensive experience of sponsor-level management of clinical trials in an academic environment.
The post-holder will establish, develop and manage a growing team of senior trial managers and data managers, each of which will work on their own portfolio of sponsored studies. The post will oversee the line management of these staff and prioritise and allocation workload to
ensure effective and efficient trial management and delivery.
The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer.
We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Daycare Unit in Kingston Hospital.
At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.
At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance.
We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.
For further information on this role, please see the attached detailed Job Description and Person Specification
Liaise closely with the CI, database programmer, statistician and other key members of the clinical trial study team (i.e. clinical fellow) to ensure on-going clinical, scientific and operational oversight.
Be a point of contact for participating sites, sponsor(s), funder(s), pharmaceutical partners, regulatory authorities and the trial oversight committees.
Oversee the day-to-day conduct of the study at participating sites, providing support and advice and addressing any logistical issues as they arise.
Organise regular meetings as needed to facilitate the efficient management of the clinical trial, preparing the agenda and meeting papers, and provide minutes following the meeting in a timely manner.
Ensure timely data collection and receipt / transfer of any clinical materials or samples for clinical trials.
This advert closes on Wednesday 8 May 2024
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