11 Data Collection jobs in the United Kingdom

The Clinical Data Standards Architect (CDSA)- Data Collection and Delivery implements and maintains efficient standard content in the data collection tools and delivery tools and defines and maintains the standard metadata supporting the data flow from data collection to data delivery.
The CDSA configures standards to the specific needs and requirements of a Therapeutic Area, compound Disease Area, generating the expected efficiencies through optimal adoption and reuse of standards. The CDSA also supports the functions adopting the standards in the clinical trials, in close collaboration with the clinical data collection team. 
The CDSA is responsible for implementing efficient standards in the Rave EDC system (Medidata Solutions). 
Responsibilities:
+ Implements the standard content in the data collections and delivery tools with the goal of creating efficiencies within the trials, consistency across the trials and automating the CRF build and the data flow from collection to SDTM.
+ Examples of standard content for the _data collection focus_
+ Standard Case Report Form Mockups 
+ Standard Questionnaires, Rating Scales and Clinical Outcome Assessments 
+ Standard Validation Rule Specifications 
+ Standard Integrations (e.g. with IWRS) 
+ Examples of standard content for the _data delivery focus_
+ Study Data Tabulation Model (SDTM)
+ Annotated Case Report Forms (CRFs)
+ Support the data transfer agreement (DTA) standards with SDTM
+ Data Review Model (DRM: internal SDTM like model)
+ Mapping metadata from data collection (CRF and DTA) to DRM
+ Mapping metadata from DRM to SDTM
+ Implements standard content in the collection and delivery tools compliant to the industry standards and health authority regulations, meeting best computer system validation practices where applicable.
+ Responsible for the correct testing and QC of the collection tools and mapping metadata and therefore collaborates with the respective functions in Integrated Data Analysis and Reporting.  
+ Defines and maintains the standard clinical data collection and the clinical data delivery standards for use in clinical trials. 
+ Maintains the data collection and delivery and metadata standards at a master level to meet additional scientific or operational requirement supporting the R&D portfolio. To that end the CDSA will guarantee formal change management control and versioning of the standards is applied and adhered to.
+ Governs formally all the changes to standards and manages multiple versions in line with adoption needs of the clinical trials and drug development programs. 
+ Pre-configures the standards in line with the specifications of the data lifecycle plans, while maintaining the traceability and lineage of the data. Documents and manages correctly the lineage between master standards and the many pre-configured standards.   
+ Provides the necessary support to the clinical data standards team and the clinical analysis team who facilitate the consistent adoption of standards in the studies (internally or outsourced to a CRO).  
+ _Data delivery focus only:_ Annotates the CRF with SDTM metadata and collaborates with his/her team members on the correctness of the annotated case report form meeting submission, scientific and operational requirements and guidelines.
Education and Experience:
+ Deep expertise in Rave EDC (Medidata Solutions) 
+ Experience with running SAS programs, coding experience preferred.
+ Experience with coding and running SAS programs
+ Knowledge of Rave EDC (Medidata Solutions)
+ Expertise with CDISC standards: SDTM, CDASH, Controlled terminology and define.xml. 
+ Experience with SAS LSAF and Pinnacle 21
+ BS/BA degree in life sciences or computer science or equivalent by work experience 
+ 2 years of relevant operational experience in clinical data management or standards
+ Relevant operational experience in clinical data standards is preferred 
+ Experience in prioritizing and managing multiple tasks simultaneously 
+ Outstanding written and verbal communication skills in English 
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Providing Project Management guidance to study teams, study startup and closeout guidance, migration support, tracking high-level study milestone information and clinical view refreshes when required in the EDC. In his/her area of responsibility, responsible to support continuous improvement framework with respect to systems deployment, project management and enhancements supported by greater partnerships with suppliers, CRO partners and industry user groups. Will have the ability to contribute to a high functioning diverse team to enable industry-leading electronic data flow. He/she will have technical expertise and significant experience gained through working with diverse and complex business processes and associated system infrastructures. May be responsible for support in systems inspection readiness and provide expertise as necessary for FDA and other health authority inspections.
Responsible for the following as well as other ad-hoc tasks.
+ Supporting study teams with scheduling migrations
+ Maintaining the Trial Data Repository in Medidata Rave
+ Database lock activities such as updating user access, clinical view (CV) refreshes
+ Database un-lock activities
+ Database archival activities such as removing all user access and turning off clinical views.
+ Uploading eCRF guidelines on the FTP server.
+ Granting user access to iMedidata and Medidata Rave
+ Submitting FTP requests for end users
+ Study Team support (internal and external partners) at a platform level for all therapeutic areas by answering ad-hoc questions.
+ Guide study team members to Data Collection Solutions documentation
+ Review listings and follow-up with study team members as appropriate
+ May have the responsibility to train or mentor new members in the organization.
+ Participate in UAT activities of system upgrades
+ Participate in cross sector initiatives as assigned
+ Assist with vendor management
+ Excellent problem solving and decision-making skills
+ Strong planning, organization and project management skills
+ Contribute to the Data Collection Solutions team active in the development, implementation, maintenance and continuous improvement of systems supporting end-to-end processes.
+ Other tasks as needed
Education and Experience Requirements/Qualifications:
+ Bachelors degree in Engineering, Science, or Computer Science is preferred.
+ Minimum of 3 years of experience working within systems covering clinical development in the Pharma sector.
+ Experience in DM lifecycle (start up - close out)
+ Standards and libraries experience
+ Knowledge of Electronic Data Capture (EDC) systems with strong working knowledge of iMedidata and Rave
+ Understanding of GCP, ICH, and 21 CFR part 11
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Job Position: Data Architect (6-Month Contract)

Role: Data Architect

Contract Duration: 6 months

IR35 Status: Outside IR35

Location: Hybrid working model based in Leeds, Manchester, or Blackpool (as required).

Start Date: ASAP

Daily Rate: Competitive

Role Summary: We are seeking a highly skilled and experienced Data Architect for a 6-month contract. The successful candidate will be responsible for designing and building data models, ensuring data integrity, and aligning data infrastructure with business requirements. This is a critical role to help shape our data strategy and ensure our systems are optimized for performance and security.

Required Experience:

• Proven experience in a Data Architect role.
• Strong knowledge of data management, modelling, and governance.
• Essential: experience with debt systems.
• Ability to work effectively with both technical and non-technical stakeholders.
• Experience in an agile environment is a plus.

How to Apply

If you are the right person for this role and have the required experience, please apply directly via the job advert.