129 Clinical Data jobs in the United Kingdom

An innovative global pharmaceutical company is looking to hire a Lead Data Manager to join them on a permanent basis. This is a full-time opportunity, open to applicants in the UK, or those with a valid right to work in the UK. Candidates must have comprehensive Lead DM experience working on complex oncology trials.

Key Responsibilities:

• Leads the collection and integration of clinical trial data from diverse sources.
• Demonstrates deep subject matter expertise in Data Management (DM), effectively supporting multiple studies with minimal supervision.
• Manages oversight of DM vendors across several studies, providing input and reviewing vendor oversight processes.
• Analyses Key Risk Indicators (KRIs) at the aggregate level (sites, regions, countries) and investigates study-level operational and patient data to identify root causes of issues.
• Delivers training and guidance to junior DM team members, serving as a subject matter expert.
• Collaborates with clinical operations, investigators, and key stakeholders to ensure seamless data flow throughout the clinical trial lifecycle.

Essential Knowledge & Experience:

• BS/BA degree in a biological science, statistics, health-related or computer science field. Advanced degree preferred or equivalent.
• Oncology experience across Phase II/III trials.
• Proficient in computer applications including database management systems, reporting tools, medical coding platforms, and Central Monitoring technologies.
• In-depth knowledge of various data sources within clinical trial settings, including expertise in handling external data types.
• Background in the pharmaceutical, clinical research, or healthcare industries, with a proven track record as a Data Manager and increasing levels of responsibility.

For a detailed discussion, please apply now with an updated CV, or contact me directly -

Advanced analytics. Intelligent insights.

IXICO plc (AIM: IXI), is a leading neuroimaging Contract Research Organization (CRO), delivering advanced Ai analytical insights in neuroscience to the global clinical trials market. Established in 2004, listed as a public company in 2013, IXICO has firmly established itself as a trusted partner to the global life sciences industry, supporting the development of new therapies for neurological conditions such as Alzheimer’s, Parkinson’s, Huntington’s Disease and Multiple Sclerosis.

With our focus on neuroscience, our purpose is to advance human health by turning data into clinically valuable insights; helping our clients reduce clinical development risk and improve return on investment from their clinical development programmes. We achieve this by combining Ai machine learning imaging biomarker analysis, together with centralised neuroimaging CRO services to provide an integrated service covering every stage of clinical development through to post-marketing surveillance. We are committed to invest in continuously enhancing our validated and peer reviewed disease optimised machine learning Ai analytics services and our infrastructure and technology to support our ambitious growth strategy. Our people are empowered to enable us to achieve our company goals and their own personal development through the “4A” values at the heart of our culture: Aspiration, Ability, Agility and Accountability.

To help us deliver our medical image analysis solutions to large clinical trials we are hiring a Associate Data Manager on a permanent full-time capacity.

Purpose of the Role:

Working closely with the Project Manager and Science Lead, the Associate Clinical Data Manager will be responsible for data cleaning and transfer of clinical neuroimaging data on a varied portfolio of neurology clinical trials.

The Associate Clinical Data Manager will ensure the data management process on each new Project is setup, quality controlled, and managed robustly; meeting regularly with the Site Manager and Image Analyst to maintain oversight of this dataflow and support with issue resolutions, as and when they arise throughout the Project. The Associate Clinical Data Manager will be the escalation point and point of contact for the Sponsor and IXICO Project Manager on all data-related questions and is directly responsible for performing data checks/reconciliations, and execution of data and image transfers.

IXICO operates its own in-house Clinical Data Management (CDM) System called TrialTrackerTM along with cutting-edge Artificial Intelligence algorithms for analysing brain scans. IXICO’s processes are tailored for managing neuroimaging data and IXICO Clinical Data Managers have the opportunity to become specialised in handling neuroimaging data within a unique CDM system.

Essential Duties and Responsibilities:

The duties and responsibilities listed below are representative, but not exhaustive of the role. There may be some variation and/or development of these duties and responsibilities without changing the general nature of the role.

• Performs data management activities, focusing on data cleaning and data transfer of imaging data sent through to IXICO for assigned projects.
• Ensure the data cleaning and transfer processes on each new project is setup, quality controlled, and managed robustly.
• Attend and participate in sponsor meetings as requested.
• Act as the escalation point and point of contact for the Sponsor and IXICO project Manager on all data related questions.
• Perform QC on all aspects of work performed in Site Management, Image Analysis and Data Management teams to ensure that data quality and integrity is maintained.
• Run and perform routine ad hoc data cleaning checks on Project data, identifying errors, inconsistencies and discrepant data for resolution.
• Track outstanding issues and following-up until resolution.
• Maintain, organize, complete, and update study documentation, including writing Data Transfer Agreements and Image Transfer Agreements and configuring associated extracts for data transfer output.
• Write project-specific transfer work instructions and perform test/production transfers.
• Assist in standardising and documenting data management procedures.
• Follow all IXICO data management (DM) procedures, policies, and work instructions.
• Read, understand, and follow applicable Standard Operating Procedures (SOPs).

Qualifications and skills required for the role:

Essential

• Bachelor’s degree in Computer Science, Life Sciences or related field preferred, or equivalent experience required.
• 1+ years’ experience of working in data management within the Pharmaceutical, Biotech or CRO industry recommended.
• Strong IT skills (working within cloud-based database systems desirable) and demonstrate experience of working with a variety of data formats.
• Experience working with Microsoft Office tools including Word and in particular Excel.
• Ability to learn other computer systems, including databases.
• Strong attention to detail and excellent communication and interpersonal skills, both verbal and written.
• Team oriented and flexible; ability to function in high volume environment with competing priorities.
• Ability to perform multiple tasks simultaneously under direction and prioritise workload.
• Ability to work independently in a group setting; ability to adjust to changing priorities.
• Maintain a professional and positive attitude.

Desirable

• SAS Experience.
• SQL Experience.

Benefits

• Competitive remuneration package including benchmarked salaries.
• Staff Annual Bonus Plans and Annual Salary Review.
• Generous employer pension contribution of 6%.
• 25 days annual leave, increasing up to 28 days with every year at IXICO.
• BUPA private medical insurance scheme.
• Life Assurance of 4x annual salary.
• Employee Benefits Portal, Perkbox offering various discounts in retail, food & drink, and entertainment.
• Engaging and social environment, with fundraising and sporting activities and seasonal events such as Summer and Christmas parties.
• Wellbeing initiatives such as eye tests, flu jabs, and Mental Health Awareness Training.
• Employee Assistance Programme offering advice and support on a wide range of topics.
• Hybrid working model pattern split between working at our vibrant head office in the City of London and remotely.
• Reimbursement allowance to purchase equipment to support working from home.
• Generous employee referral scheme offering £2,000 for referring a successful candidate to the company.
• Financial assistance for professional qualifications.
• A company in an industry where your work has an impact every single day.

How to Apply

IXICO is working hard to create a representative, inclusive and empowered team, because we believe different experiences, perspectives and backgrounds make a better workplace, and ultimately better services.

IXICO doesn’t discriminate on the basis of race, colour, religion or belief, gender, national origin, age, sexual orientation, marital status, disability or any other protected class.

This is a great opportunity for a motivated Associate Data Manager in a permanent full-time capacity to thrive in an engaging and fast-paced environment, to make a difference on an everyday basis.

If you think IXICO should meet you, please send us your CV and covering letter by email to or apply directly via LinkedIn . We are looking forward to your application.

Please note that our entire business is operating under a Hybrid-Working Model , where UK-based employees are required to attend our London office 2 days a week . If you have got any questions, please reach out to our careers team.

Please note that IXICO will process the data provided by you only in order to perform the outlined recruitment exercise. For more details on what data we process and on what legal basis this happens please view our Recruitment Privacy Policy or contact

Data Management Lead | Global Pharma | UK-Based (Remote) | Full-Time

We're partnered with a leading global pharma company who are seeking a Data Management Lead to support their innovative clinical development pipeline.

This is a hands-on, high-impact role where you'll take ownership of data management activities across multiple studies, from study start-up to closeout. You’ll be the primary DM contact in study teams, leading everything from database build to vendor oversight, while collaborating closely with Clinical Operations, Programming, and external partners.

What You'll be Doing:

• Lead and oversee all DM activities across assigned studies
• Represent DM in cross-functional study and project teams
• Ensure high-quality, regulatory-compliant data deliverables
• Manage CROs and external vendors
• Review and support central monitoring efforts
• Mentor junior team members and share DM expertise

What we're Looking for:

• Strong clinical DM background with experience across full study life cycle
• Proven ability to manage multiple studies and vendors simultaneously
• Good grasp of eSource, external data, medical coding, central monitoring tools
• Industry experience in pharma, CRO or health-related fields
• Based in the UK with flexibility to visit the office once per quarter
• Life Science or Computer Science Degree preferred

What to do next?

Apply now with your CV to avoid missing out on this opportunity!

Job Title: Clinical Trials Manager

Location: London

Contract: 5 months

Hours: 14.5 hours per week (9-5 Mondays/Tuesday)

Rates: 22.79-23.97 p/h

Job Description

SRG are looking for a clinical trials manager to join a leading higher educations provider based in London. The primary role of the post holder is to set up and support a high quality clinical trial at the CCTU.

Duties and Responsibilities

• To establish and maintain effective management systems for the trial
• To act as the central Trials Unit contact for the Trial
• To work closely with the Chief Investigator, trial and IT staff to ensure the successful management of the Trial.
• Secure all necessary approvals for the trial and participating sites according to the UK regulations including UK Research Governance Framework
• Coordinate the design, printing and distribution of trial documentation
• Develop trial specific documentation that is compliant with the CCTU Policies and Standard Operating Procedures (SOPs) and ensure this is implemented and kept up to date.
• Ensure sites have appropriate training and maintain necessary records.
• Work within budget constraints in liaison with the Project Manager.
• Ensure that good communication is maintained between the CCTU and recruiting centre staff
• Provide updates on the progress of the trial at regular Trial Management Group meetings, to the Independent Data Monitoring and Trial Steering Committees and to the funder as required.
• Monitor the trial sites to assess compliance with the protocol and regulatory requirements.
• Prepare under the guidance of the Clinical Project Manager, the trial specifications for the Database.
• Undertake Risk Assessment of the trial and, with the Clinical Project Manager, propose appropriate mitigations.
• Minute trial related meetings.
• Supervise the data collected and enter data if required.
• Supervise the data cleaning and validation, including querying and chasing missing data in a timely manner.
• Monitor trial recruitment, providing support and motivation to recruiting staff as required.
• Ensure the timely submission and processing of data and documents from sites to the CTU including safety events. Prepare and submit the necessary reports to appropriate regulatory, ethical and other parties (such as submission of safety reports to the Ethics Committee).
• Represent the trial at conferences, meetings and internal unit meetings as appropriate.
• Keep the relevant literature searches up to date.
• Participate in university and the CCTU training and development initiatives.
• Carry out any other comparable tasks as required including being prepared to assist those working on other studies/trials as directed by the Head of Clinical Trial Operations.

Experience and Qualifications

• Degree and/or equivalent experience in Clinical Trials
• Experience of managing a clinical trial
• Experience of managing a trial of an investigational medicinal product
• Comprehensive understanding of UK Clinical Trials Regulations, ICH Good Clinical Practice, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health's Research Governance Framework
• Experience of monitoring
• Experience of using Pharmacovigilance systems
• Experience of working in an academic or similar institution
• Experience of public speaking and giving presentations
• Experience of data management
• Evidence of ability to set up and maintain effective management system in trials
• Excellent IT skills; MS Office Suite, Trial Databases and other Trial related systems (such as IMP management, Randomisation)
• Excellent communication and interpersonal skills
• A methodical and accurate approach to work with attention to detail
• The ability to make and carry out decisions and know when to confer with colleagues or refer matters onwards
• The ability to work without direct supervision; to manage own workload and display good organisational ability
• Take responsibility for setting and meeting targets for your own work and others
• Ability to evaluate risks inherent in clinical trials and decide those which should be prioritised to ensure that risks are properly managed
• Advanced organisational skills, managing several projects that are often time pressured, concurrently
• Ability to supervise other members of the team, promote good working relationships and resolve difficult situations
• Commitment to and knowledge of advancing equality, diversity and inclusion

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: Clinical Trials Manager

Location: London

Contract: 5 months

Hours: 14.5 hours per week (9-5 Mondays/Tuesday)

Rates: 22.79-23.97 p/h

Job Description

SRG are looking for a clinical trials manager to join a leading higher educations provider based in London. The primary role of the post holder is to set up and support a high quality clinical trial at the CCTU.

Duties and Responsibilities

• To establish and maintain effective management systems for the trial
• To act as the central Trials Unit contact for the Trial
• To work closely with the Chief Investigator, trial and IT staff to ensure the successful management of the Trial.
• Secure all necessary approvals for the trial and participating sites according to the UK regulations including UK Research Governance Framework
• Coordinate the design, printing and distribution of trial documentation
• Develop trial specific documentation that is compliant with the CCTU Policies and Standard Operating Procedures (SOPs) and ensure this is implemented and kept up to date.
• Ensure sites have appropriate training and maintain necessary records.
• Work within budget constraints in liaison with the Project Manager.
• Ensure that good communication is maintained between the CCTU and recruiting centre staff
• Provide updates on the progress of the trial at regular Trial Management Group meetings, to the Independent Data Monitoring and Trial Steering Committees and to the funder as required.
• Monitor the trial sites to assess compliance with the protocol and regulatory requirements.
• Prepare under the guidance of the Clinical Project Manager, the trial specifications for the Database.
• Undertake Risk Assessment of the trial and, with the Clinical Project Manager, propose appropriate mitigations.
• Minute trial related meetings.
• Supervise the data collected and enter data if required.
• Supervise the data cleaning and validation, including querying and chasing missing data in a timely manner.
• Monitor trial recruitment, providing support and motivation to recruiting staff as required.
• Ensure the timely submission and processing of data and documents from sites to the CTU including safety events. Prepare and submit the necessary reports to appropriate regulatory, ethical and other parties (such as submission of safety reports to the Ethics Committee).
• Represent the trial at conferences, meetings and internal unit meetings as appropriate.
• Keep the relevant literature searches up to date.
• Participate in university and the CCTU training and development initiatives.
• Carry out any other comparable tasks as required including being prepared to assist those working on other studies/trials as directed by the Head of Clinical Trial Operations.

Experience and Qualifications

• Degree and/or equivalent experience in Clinical Trials
• Experience of managing a clinical trial
• Experience of managing a trial of an investigational medicinal product
• Comprehensive understanding of UK Clinical Trials Regulations, ICH Good Clinical Practice, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health's Research Governance Framework
• Experience of monitoring
• Experience of using Pharmacovigilance systems
• Experience of working in an academic or similar institution
• Experience of public speaking and giving presentations
• Experience of data management
• Evidence of ability to set up and maintain effective management system in trials
• Excellent IT skills; MS Office Suite, Trial Databases and other Trial related systems (such as IMP management, Randomisation)
• Excellent communication and interpersonal skills
• A methodical and accurate approach to work with attention to detail
• The ability to make and carry out decisions and know when to confer with colleagues or refer matters onwards
• The ability to work without direct supervision; to manage own workload and display good organisational ability
• Take responsibility for setting and meeting targets for your own work and others
• Ability to evaluate risks inherent in clinical trials and decide those which should be prioritised to ensure that risks are properly managed
• Advanced organisational skills, managing several projects that are often time pressured, concurrently
• Ability to supervise other members of the team, promote good working relationships and resolve difficult situations
• Commitment to and knowledge of advancing equality, diversity and inclusion

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

An exciting opportunity to join Veramed's Data Management Business Unit! As we continue to grow and build on our success, we're looking to recruit a passionate and driven Senior Clinical Data Manager. You'll be required to have strong and indepth expereince of Data Management Study Start Up, Medidata Rave (including eCOA) and experience of vendor management. This role can be based in our UK offices or a hybrid working model.

Veramed prides itself on two key areas: providing the highest quality Data Management, Statistics and Programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth.

Purpose:

The role of the Senior Clinical Data Manager is to provide data management support to the data management department across a range of projects, sponsors and therapeutic areas. Provide expertise and manage the start up of new data management studies.

Key Responsibilities:

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.

Technical:

• Review of clinical protocols
• Create or review Case Report Forms for data collection and compare with the protocol to ensure consistency
• Create or review Edit Check Specification document
• Preparation of UAT documentation and perform UAT of EDC and communication of findings
• Creation of study specific documents such as Data Management Plan, Data Review Plan, eCRF Completion Guidelines, etc.
• Create or review specifications for data review listings and / or customized reports to facilitate data cleaning
• Ongoing review of data entered in EDC to ensure the data is clean for analysis
• Issue queries to clinical monitors or investigational sites as appropriate
• Resolve standard queries
• Perform medical coding
• Work with external vendors on data transfer agreements / specifications
• Ensure external data is reconciled as required
• Track queries and data cleaning activities to ensure ongoing review of data entered is completed and data is fit for analysis.
• Maintain study master file documents and any other documents that are required to be audit ready
• Work in accordance with internal (or sponsor, where applicable) SOPs and procedures

Project Management:

• May serve as the main contact for the sponsor
• Awareness of study budget and proactive identification of scope changes
• Ensure key project milestones are delivered on time with the highest quality
• Maintain timelines and communicate risks / updates to the Data Management Project Manager
• Collaborate with cross-functional team members to ensure that the study deliverables are provided on time and with quality

General:

• Lead internal and client study team meetings effectively
• Present study updates internally and at sponsor meetings
• Share scientific, technical and practical knowledge within the team and with colleagues
• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
• Build effective collaborative working relationships with internal and sponsor team members
• Seek opportunities to develop innovative ideas and sharing when appropriate
• Mentorship of more junior team members
• Contribution to development of internal training materials
• Contribution to internal process improvement initiatives

Minimum Qualification Requirements

• BSc or MSc in numerical discipline (or relevant equivalent industry experience).
• At least 7 years of relevant industry experience.
• Understanding of clinical drug development process, relevant disease areas, endpoints, and different study designs
• Awareness of industry and project standards & ICH guidelines
• Excellent verbal and written communication skills
• Interpersonal/teamwork skills for effective interactions
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables
• Demonstrated problem solving ability and attention to detail
• Project leadership experience
• Ability to make informed and appropriate decisions

Your new company
A leading biotech company, with a well-established presence in multiple therapy areas is looking to hire a Lead Statistical Genetics Scientist to support the further development of their products.They have a track record of innovation and a highly collaborative, cross-functional work environment.You would be joining an established team with significant expertise within genetics an.

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