Job summary
The Late Phase Oncology (LPO) data management team is responsible for the accurate and complete capture of detailed clinical trial research data from the medical records. These data sets are used to determine whether promising new anti-cancer treatments merit further development.
Main duties of the job
? Manage own caseload of trial data management.? Interpret and extract data from the source medical records to paper or electronic case report forms as required by the trial protocol and other applicable instruction.? Ensure accuracy, completeness, consistency and compliance with study guidelines of source documents, CRFs, and related documents as an essential part of the research effort.? Receive data queries, liaising with responsible clinical research staff and monitors as necessary to resolve any missing or discrepant data and respond to the originator.? Resolve discrepancies by referring to and interpreting the trial protocols whenever required by trial management monitors or investigators.? Liaise with the consultant principal investigator (PI) or delegated doctor, allocated research nurse, and sponsor company monitor for resolving complicated queries.? Writing standard follow-up requests to GPs, referring clinicians? Liaise with data managers, clinicians and nurses to produce forms for use during patient interviews and assessments.? Prepare and submit progress reports to the senior data manager, investigators and sponsors.? Be aware of and adhere to all Trust and locally agreed policies or SOPs? Be responsible for own professional
We are a diverse research team looking for an individual who can work in the a friendly data team.
Closing date and time: 18th December 2023 Midnight
About us
Oxford University Hospitals NHS Foundation Trustis one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. Find out more here www.ouh.nhs.uk
The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury.
Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via theOUH YouTube channel
Job description
Job responsibilities
Manage own caseload of trial data management. Interpret and extract data from the source medical records to paper or electronic case report forms as required by the trial protocol and other applicable instruction. Ensure accuracy, completeness, consistency and compliance with study guidelines of source documents, CRFs, and related documents as an essential part of the research effort. Receive data queries, liaising with responsible clinical research staff and monitors as necessary to resolve any missing or discrepant data and respond to the originator. Resolve discrepancies by referring to and interpreting the trial protocols whenever required by trial management monitors or investigators. Liaise with the consultant principal investigator (PI) or delegated doctor, allocated research nurse, and sponsor company monitor for resolving complicated queries. Writing standard follow-up requests to GPs, referring clinicians Liaise with data managers, clinicians and nurses to produce forms for use during patient interviews and assessments. Prepare and submit progress reports to the senior data manager, investigators and sponsors. Be aware of and adhere to all Trust and locally agreed policies or SOPs Be responsible for own professional
Job description
Job responsibilities
Manage own caseload of trial data management. Interpret and extract data from the source medical records to paper or electronic case report forms as required by the trial protocol and other applicable instruction. Ensure accuracy, completeness, consistency and compliance with study guidelines of source documents, CRFs, and related documents as an essential part of the research effort. Receive data queries, liaising with responsible clinical research staff and monitors as necessary to resolve any missing or discrepant data and respond to the originator. Resolve discrepancies by referring to and interpreting the trial protocols whenever required by trial management monitors or investigators. Liaise with the consultant principal investigator (PI) or delegated doctor, allocated research nurse, and sponsor company monitor for resolving complicated queries. Writing standard follow-up requests to GPs, referring clinicians Liaise with data managers, clinicians and nurses to produce forms for use during patient interviews and assessments. Prepare and submit progress reports to the senior data manager, investigators and sponsors. Be aware of and adhere to all Trust and locally agreed policies or SOPs Be responsible for own professional
Person Specification
Criteria
Essential
- Educated to A-Level or equivalent
- IT skills
- Communication skills
Desirable
- Research experience
- Experience with EPR
- GCP
Person Specification
Criteria
Essential
- Educated to A-Level or equivalent
- IT skills
- Communication skills
Desirable
- Research experience
- Experience with EPR
- GCP
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
