63 Clinical Systems jobs in the United Kingdom

Our client is a biopharmaceutical organization developing next-generation T cell therapies to treat cancer and autoimmune diseases. Their innovative cell programming technologies enable precisely targeted, highly active treatments designed to improve patient outcomes. We are currently seeking a Clinical Systems Specialist to join their team on a contract basis.

Role Summary

We are seeking a highly skilled and organized Clinical Systems Specialist to support the management and functionality of clinical systems and processes. The ideal candidate will be responsible for ensuring the smooth management of user access, performing system validation, and collaborating with cross-functional teams for system updates, releases, and configuration changes. This role will support the review of release notes, contribute to UAT processes and manage system configurations and updates related to clinical studies.

Key Responsibilities

User Management & Access Control:

· Create and manage User Management Forms for system users.

· Oversee the granting and revocation of user access rights, ensuring compliance with organizational protocols and security standards.

· Run monthly user rights reports and handle any accounts new or to be disabled.

· Ensure that user roles and permissions are correctly assigned across systems and modules.

System Validation:

· Support the review of Release Notes for system changes, including assessing impact and ensuring proper implementation across relevant systems and modules.

· Support the User Acceptance Testing (UAT) and document creation collaborating with the IT

and CSV team.

· Support the end user training.

· Support on the implementation of any new modules, systems and configurations on current systems.

· Perform system validation tasks to ensure that clinical systems operate according to specified requirements and regulatory guidelines.

· Collaborate with the IT and CSV teams to support User Acceptance Testing (UAT), ensuring that changes meet functional and technical requirements.

Study and Site Management:

· Add new clinical study, country, sites, Principal Investigators (PIs), Sub-Investigators (Sub Is), participants, vendors into the clinical system as necessary.

· Update and maintain accurate CSV entries to reflect the most current information.

· Create, review, and maintain templates and wizard configurations in the clinical system to ensure accuracy and compliance with study protocols.

· Provide ongoing support for system changes and upgrades, working with teams to ensure system functionality aligns with operational needs.

· Provide support to study teams for document uploads and QC, as required

Demonstrated skills and competencies

E – Essential

P – Preferred

Experience: Knowledge of system validation and UAT processes (E)

Experience with Clinical Trial Management Systems (CTMS), eTMF, Electronic Data Capture (EDC), RAVE, Medidata (E)

Experience in a clinical or system management role, preferably in the clinical trials or healthcare industry (P)

Qualifications

Bachelors or Masters Degree (E) in Science (P)

Skills/Specialist knowledge

Strong attention to detail.

Ability to collaborate effectively across teams

Excellent communication skills, both written and verbal.

Proficiency in Microsoft Office and other relevant software.

Our client is a biopharmaceutical organization developing next-generation T cell therapies to treat cancer and autoimmune diseases. Their innovative cell programming technologies enable precisely targeted, highly active treatments designed to improve patient outcomes. We are currently seeking a Clinical Systems Specialist to join their team on a contract basis.

Role Summary

We are seeking a highly skilled and organized Clinical Systems Specialist to support the management and functionality of clinical systems and processes. The ideal candidate will be responsible for ensuring the smooth management of user access, performing system validation, and collaborating with cross-functional teams for system updates, releases, and configuration changes. This role will support the review of release notes, contribute to UAT processes and manage system configurations and updates related to clinical studies.

Key Responsibilities

User Management & Access Control:

· Create and manage User Management Forms for system users.

· Oversee the granting and revocation of user access rights, ensuring compliance with organizational protocols and security standards.

· Run monthly user rights reports and handle any accounts new or to be disabled.

· Ensure that user roles and permissions are correctly assigned across systems and modules.

System Validation:

· Support the review of Release Notes for system changes, including assessing impact and ensuring proper implementation across relevant systems and modules.

· Support the User Acceptance Testing (UAT) and document creation collaborating with the IT

and CSV team.

· Support the end user training.

· Support on the implementation of any new modules, systems and configurations on current systems.

· Perform system validation tasks to ensure that clinical systems operate according to specified requirements and regulatory guidelines.

· Collaborate with the IT and CSV teams to support User Acceptance Testing (UAT), ensuring that changes meet functional and technical requirements.

Study and Site Management:

· Add new clinical study, country, sites, Principal Investigators (PIs), Sub-Investigators (Sub Is), participants, vendors into the clinical system as necessary.

· Update and maintain accurate CSV entries to reflect the most current information.

· Create, review, and maintain templates and wizard configurations in the clinical system to ensure accuracy and compliance with study protocols.

· Provide ongoing support for system changes and upgrades, working with teams to ensure system functionality aligns with operational needs.

· Provide support to study teams for document uploads and QC, as required

Demonstrated skills and competencies

E – Essential

P – Preferred

Experience: Knowledge of system validation and UAT processes (E)

Experience with Clinical Trial Management Systems (CTMS), eTMF, Electronic Data Capture (EDC), RAVE, Medidata (E)

Experience in a clinical or system management role, preferably in the clinical trials or healthcare industry (P)

Qualifications

Bachelors or Masters Degree (E) in Science (P)

Skills/Specialist knowledge

Strong attention to detail.

Ability to collaborate effectively across teams

Excellent communication skills, both written and verbal.

Proficiency in Microsoft Office and other relevant software.

Our client is a biopharmaceutical organization developing next-generation T cell therapies to treat cancer and autoimmune diseases. Their innovative cell programming technologies enable precisely targeted, highly active treatments designed to improve patient outcomes. We are currently seeking a Clinical Systems Specialist to join their team on a contract basis.

Role Summary

We are seeking a highly skilled and organized Clinical Systems Specialist to support the management and functionality of clinical systems and processes. The ideal candidate will be responsible for ensuring the smooth management of user access, performing system validation, and collaborating with cross-functional teams for system updates, releases, and configuration changes. This role will support the review of release notes, contribute to UAT processes and manage system configurations and updates related to clinical studies.

Key Responsibilities

User Management & Access Control:

· Create and manage User Management Forms for system users.

· Oversee the granting and revocation of user access rights, ensuring compliance with organizational protocols and security standards.

· Run monthly user rights reports and handle any accounts new or to be disabled.

· Ensure that user roles and permissions are correctly assigned across systems and modules.

System Validation:

· Support the review of Release Notes for system changes, including assessing impact and ensuring proper implementation across relevant systems and modules.

· Support the User Acceptance Testing (UAT) and document creation collaborating with the IT

and CSV team.

· Support the end user training.

· Support on the implementation of any new modules, systems and configurations on current systems.

· Perform system validation tasks to ensure that clinical systems operate according to specified requirements and regulatory guidelines.

· Collaborate with the IT and CSV teams to support User Acceptance Testing (UAT), ensuring that changes meet functional and technical requirements.

Study and Site Management:

· Add new clinical study, country, sites, Principal Investigators (PIs), Sub-Investigators (Sub Is), participants, vendors into the clinical system as necessary.

· Update and maintain accurate CSV entries to reflect the most current information.

· Create, review, and maintain templates and wizard configurations in the clinical system to ensure accuracy and compliance with study protocols.

· Provide ongoing support for system changes and upgrades, working with teams to ensure system functionality aligns with operational needs.

· Provide support to study teams for document uploads and QC, as required

Demonstrated skills and competencies

E – Essential

P – Preferred

Experience: Knowledge of system validation and UAT processes (E)

Experience with Clinical Trial Management Systems (CTMS), eTMF, Electronic Data Capture (EDC), RAVE, Medidata (E)

Experience in a clinical or system management role, preferably in the clinical trials or healthcare industry (P)

Qualifications

Bachelors or Masters Degree (E) in Science (P)

Skills/Specialist knowledge

Strong attention to detail.

Ability to collaborate effectively across teams

Excellent communication skills, both written and verbal.

Proficiency in Microsoft Office and other relevant software.

About the Company We change lives by transforming health and care.Established in 2006, we are one of the UK's leading independent providers of community health and care services, working with health and care commissioners and communities to transform services with a focus on experience, efficiency and improved outcomes. We deliver and transform adult and children community health services, primary care services including urgent care, sexual health, dermatology and MSK services as well as adult social care and wellbeing services. Across England, we support communities of many millions and directly help more than half a million people each year - guided by our simple values: we care, we think, we do.We're committed to equal opportunities and welcome applications from a broad, diverse range of people who want to join our team. We’re a Disability Confident Committed company, so we work to provide facilities, work environment adjustments and technical solutions to be as inclusive of everyone.While it doesn’t happen often, sometimes a role is very popular, and we’ll need to close it earlier than the date we’ve shown here. If you’re keen to join our team, we’d love to hear from you so please apply as soon as you can.As you’d expect, safeguarding and protecting the children, young people and vulnerable adults that we work with is of the utmost importance so we have policies and procedures in place to promote safeguarding and safer working practices and everyone who joins the team is subject to a safer recruitment process, including the disclosure of criminal records and vetting checks.Finally, we need to let you know that the company you’ll work for is part of HCRG Care Group Holdings Limited and by applying for this job we’ll need to process and hold information about you. If you would like to know a little more about how we use your information, please see our website's privacy policy.

Are you ready to shape the future of data in financial services? We’re looking for a passionate Data Management Specialist to help drive our enterprise-wide data transformation.

In this exciting role, you’ll be at the heart of delivering our Data Strategy, leading on the rollout of Purview, enhancing our Data Management capabilities, supporting the rollout of Microsoft Fabric. You’ll work within a fast-paced, collaborative environment to embed best-in-class data practices and governance across the business.

This is a hybrid role with some presence required at our Bournemouth office. This role is a Fixed Term Contract for 12 months.

Key Responsibilities

•Spearheading the development of our Data Management roadmap, introducing key capabilities like Metadata Management, Master Data Management, Data Lineage, Business Glossaries, and Data Dictionaries.
•Strengthening our Data Ownership and Stewardship communities and championing our Data Literacy programme.
•Collaborating with the IT communities, Data Office and Data Privacy function to ensure data quality, consistency, and compliance across all business lines.
•Leading the implementation of Purview and supporting the migration to Microsoft Fabric, ensuring sensitive data is protected and risks are mitigated.
•Partner with the Head of Data, Data Governance Lead and Data Quality Lead to build a high-impact Data Governance team.
•Define and implement data management strategies aligned with regulatory frameworks (e.g., GDPR, BCBS 239).
•Act as a technical advisor and coach for our Accountable Executives, Data Owners and Stewards, delivering training and guidance.
•Drive MDM initiatives and collaborate with SCV Engineers to deliver a unified customer view.
•Conduct audits, support data migration, and ensure robust data classification and retention practices.

About You
Essential:
•Proven experience in data management/governance preferably within Financial Services.
•Hands-on implementation experience with tools like Purview, Collibra, Informatica, or Alation. 
•Solid SQL skills and familiarity with Azure, Fabric, or other cloud platforms.
•Knowledge of data privacy regulations (UK GDPR, Data Protection Act 2018) and ETL processes.

Desirable:
•Purview implementation experience.
•Certifications such as DAMA/CDMP.
•Experience in data remediation, migration, and quality improvement projects.
•Ability to work cross-functionally with IT, compliance, and business teams.

We’re proud of our inclusive culture at LV= and, as an equal-opportunity employer, we continually work to remove unconscious bias from our recruitment process. We value our colleagues for what they bring to our team regardless of any protected status or characteristics they may have. Talk to us about flexible working as part of your application; if it’s right for you, our members and customers, and our business, then we’ll do everything we can to make it happen.

Please note that we are unable to offer Skilled Worker Visa Sponsorship for this role. Therefore, you must ensure that you are eligible to work in the UK without our sponsorship in order for your application to be considered.

Community Advisor (French Speaker)

Start Date: Immediate

Duration: Long-term Project

Hours: 10 hours per week

Location: Remote

About the Role

Key Responsibilities

• Provide strategic direction, best practices, and guidance to ensure communities align with business objectives
• Define the community’s mission, vision, and goals
• Advise on optimal interaction styles and community structures
• Establish KPIs and reporting frameworks to measure success
• Identify and nurture superusers, ambassadors, and influencers
• Provide insights into platform trends, industry best practices, and product roadmaps
• Act as a liaison between customer stakeholders and internal teams

Skills & Experience

• Experience with data analysis using tools such as Google Sheets and in-product analytics tools
• Skilled at creating data-centered reports using Google Slides
• Ability to research technical product details (supported by AI documentation) and help resolve community issues
• Basic understanding of community forums and online engagement best practices
• Strong analytical and strategic thinking skills able to form actionable recommendations based on community insights
• Excellent rapport-building and communication skills
• Proactive , organised, and solution-oriented

This role offers flexibility, autonomy, and the chance to influence thriving online communities for a global audience. If you’re a data-savvy, community-minded professional who’s fluent in French, we’d love to hear from you!