The post holder will work as part of a team of data management/study coordination staff providing comprehensive data management and trial coordination support to the department.
Responsibilities will include ensuring that clinical data required for CRF adopted trials are completed, validated, and returned to study sponsors in an accurate and timely fashion, promoting high quality research, both within the Trust, nationally and internationally.
The post holder will work as part of a team that provides the focal point for information requests and queries within the department. The post holder will ensure the clinical data collection, entry, and transfer of information is of the highest standard and will be expected to be part of a team which develops the existing data storage systems and processes associated with them, as the needs of the service change.
The post is part of a team of data and study coordination staff in the CRF, and as such, the post holder will be expected to work as part of this team, providing cover for other members of the team when necessary and working together to proactively improve data management within the department.
The NIHR Moorfields Clinical Research Facility (‘CRF’) requires a Data Officer to join the Research Operations Team.
The post holder should have a keen interest in the data acquisition and coordination of Clinical Research.
At Moorfields, we provide more than just an excellent career and great colleagues to work with. We also offer:
Salary including High-Cost Area Supplement Opportunity to join the NHS Pension Scheme Free 24/7 independent counselling service Learning and development opportunities Easy and quick transport links A range of attractive benefits and discounts Access to Blue Light Card and other NHS Discount Schemes Free Pilates classes Full support and training to develop your skills Flexible working friendly organisation Ensure effective data and data quality management, and reporting for studies undertaken within the Clinical Research Facility.
To maintain records of accrual to trials.
To effectively manage database information, and maintain patient lists and databases for designated studies.
Responsible for ensuring the accurate and timely capture of clinical data from source, in compliance with standard operating procedures and study protocols.
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Responsibilities will include ensuring that clinical data required for CRF adopted trials are completed, validated, and returned to study sponsors in an accurate and timely fashion, promoting high quality research, both within the Trust, nationally and internationally.
The post holder will work as part of a team that provides the focal point for information requests and queries within the department. The post holder will ensure the clinical data collection, entry, and transfer of information is of the highest standard and will be expected to be part of a team which develops the existing data storage systems and processes associated with them, as the needs of the service change.
The post is part of a team of data and study coordination staff in the CRF, and as such, the post holder will be expected to work as part of this team, providing cover for other members of the team when necessary and working together to proactively improve data management within the department.
The NIHR Moorfields Clinical Research Facility (‘CRF’) requires a Data Officer to join the Research Operations Team.
The post holder should have a keen interest in the data acquisition and coordination of Clinical Research.
At Moorfields, we provide more than just an excellent career and great colleagues to work with. We also offer:
Salary including High-Cost Area Supplement Opportunity to join the NHS Pension Scheme Free 24/7 independent counselling service Learning and development opportunities Easy and quick transport links A range of attractive benefits and discounts Access to Blue Light Card and other NHS Discount Schemes Free Pilates classes Full support and training to develop your skills Flexible working friendly organisation Ensure effective data and data quality management, and reporting for studies undertaken within the Clinical Research Facility.
To maintain records of accrual to trials.
To effectively manage database information, and maintain patient lists and databases for designated studies.
Responsible for ensuring the accurate and timely capture of clinical data from source, in compliance with standard operating procedures and study protocols.
#J-18808-Ljbffr
