429 Clinical Data Manager jobs in the United Kingdom

Our client is a leading pharmaceutical research organization seeking a meticulous and experienced Remote Clinical Data Manager to oversee the collection, validation, and management of clinical trial data. This is a fully remote position, offering the flexibility to work from anywhere within the UK. You will be responsible for ensuring the quality, integrity, and accuracy of data generated from global clinical studies, adhering to strict regulatory guidelines such as GCP, ICH, and FDA regulations. Your core duties will include developing data management plans, designing electronic data capture (EDC) systems, establishing data validation checks, and managing data cleaning activities. You will collaborate closely with clinical operations teams, biostatisticians, and programming groups to ensure timely database lock. The ideal candidate will have a strong understanding of the clinical trial process, robust data management principles, and proficiency in EDC systems and clinical data management software. Excellent attention to detail, strong analytical skills, and the ability to work independently and manage multiple projects simultaneously are essential for this role. You will play a critical role in ensuring the reliability of data that forms the basis of crucial therapeutic advancements. This position offers an exciting opportunity to contribute to groundbreaking pharmaceutical research from the comfort of your home office.

Responsibilities:

• Develop and implement clinical data management plans (DMPs).
• Design, build, and validate Electronic Data Capture (EDC) databases.
• Oversee data entry, query generation, and data cleaning processes.
• Ensure data accuracy, completeness, and integrity in compliance with protocols.
• Manage database lock procedures in collaboration with cross-functional teams.
• Perform data reviews and quality checks throughout the study lifecycle.
• Contribute to the development of data standards and best practices.
• Maintain study documentation related to data management.
• Ensure adherence to regulatory requirements (GCP, ICH, FDA).
• Provide support and training to site staff on data collection procedures.

Qualifications:

• Bachelor's degree in a life science, computer science, statistics, or a related field.
• Minimum of 5 years of experience in clinical data management within the pharmaceutical or biotech industry.
• Proven experience with EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva Vault EDC).
• Strong understanding of clinical trial processes and data management lifecycles.
• Knowledge of CDISC standards (SDTM, ADaM) is highly desirable.
• Proficiency in data analysis and quality control techniques.
• Excellent communication, organizational, and problem-solving skills.
• Ability to manage multiple projects and meet strict deadlines in a remote setting.
• Familiarity with regulatory guidelines (GCP, ICH).
• Self-motivated and able to work autonomously.

The CDM will perform scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).
Deliverables:
- Services rendered will adhere to applicable Client SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc.
- Provides scientific data review support for more than one low to moderate complexity trial or one high complexity trial.
- The data management expert who, within the therapeutic area, is performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS). Tapping into technical and clinical expertise, closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study. Reviews all necessary data flows, the Data Management Plans and performs continuous (complex) data review activities on the studies in the assigned program.
- Involved in study related activities from the protocol design stage onwards, providing input into the study specific and/or indication specific data collection tools.
- Reviews (complex) scientific study data, manages CDM and SRS/SRP related queries in eDC system and holds discussions with SRS/SRP. Involvement in other review activities (e.g., Coding, SAE reconciliation) is possible. Leads and/or attends meetings as appropriate.
- Takes a leadership role with SRP/SRS and collaborates with the GDM to establish, align and confirm scientific clinical data review expectations for assigned trial(s).
- With the trial customer, CRO and other functional partners in relation to CDM related activities:
o Reviews content and integration requirements for eCRF and other data collection tools
o Establishes conventions and quality expectations for clinical data.
o Set timelines and follow‐up regularly to ensure delivery of all Clinical Data Management milestones
- Creates the Integrated Review Plan ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Reviews related clinical data management documents. Ensures compliance with regulatory guidelines and documentation requirements.
- Ensures real‐time inspection readiness of all assigned deliverables for the trial; participate in Regulatory Agency inspection and Client internal audits as necessary.
- Plans and tracks applicable CDM deliverables. Ensures CDM deliverables are on time.
- Takes a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are met.
- Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level.
- Identifies and participates in process, system, and tool improvement initiatives within clinical data management.
Therapeutic Area - Oncology, Cardiovascular and Immunology
**Education/Experience**
- BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
- 5 years Data management experience. Data Management experience preferably including clinical data review or significant experience with clinical data review. Knowledge in medical terminology would be preferable
- Collaboration with Clinical teams.
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

A leading pharmaceutical research company is looking for an experienced and highly organized Remote Lead Clinical Data Manager to oversee and ensure the quality and integrity of clinical trial data. This is a fully remote position, offering the flexibility to work from any location. The Lead Clinical Data Manager will be responsible for managing all aspects of clinical data collection, validation, and database lock for multiple studies. You will lead a team of data managers, providing guidance, training, and performance feedback, while ensuring adherence to strict regulatory guidelines (e.g., GCP, CDISC standards) and company SOPs.

Key responsibilities include developing data management plans, designing data collection tools (e.g., EDC systems), performing data validation checks, resolving data queries, and managing the data

Our client, a leading pharmaceutical innovator, is seeking a highly experienced Senior Clinical Data Manager to join their dedicated research team. This position is fully remote, allowing you to contribute to critical drug development from the comfort of your home. You will be responsible for the end-to-end management of clinical trial data, ensuring data quality, integrity, and compliance with regulatory standards (e.g., GCP, ICH guidelines). Your core duties will involve designing Case Report Forms (CRFs), developing data management plans, establishing database specifications, and performing data validation checks. You will lead data cleaning activities, manage data reconciliation processes, and ensure timely database lock. This role requires extensive experience with Electronic Data Capture (EDC) systems and a deep understanding of clinical trial processes. You will collaborate closely with clinical operations, biostatistics, and regulatory affairs teams to ensure the seamless integration of data management into the overall trial execution. A key aspect of this role is ensuring that all data activities are meticulously documented and auditable. You will also be involved in selecting and managing EDC vendors and ensuring adherence to contractual agreements. The ideal candidate will possess strong leadership qualities, excellent attention to detail, and the ability to manage multiple complex clinical trials concurrently. You should be adept at identifying and mitigating data-related risks and implementing process improvements. Experience with CDISC standards (SDTM, ADaM) is essential. This is a vital role in bringing life-saving therapies to patients, requiring a commitment to excellence and a proactive approach to data management challenges. Your contributions will be crucial in supporting the successful progression of our client's pharmaceutical pipeline.
Responsibilities:

• Oversee and manage all aspects of clinical trial data management.
• Develop and implement comprehensive data management plans (DMPs).
• Design and manage Case Report Forms (CRFs) and eCRFs.
• Perform data validation and query resolution using EDC systems.
• Ensure data integrity, quality, and compliance with regulatory standards.
• Lead database lock activities for clinical studies.
• Collaborate with clinical, statistical, and regulatory teams.
• Manage data management vendors and CROs.
• Ensure all data management activities are thoroughly documented.
• Contribute to the development and implementation of data management SOPs.

Qualifications:

• Bachelor's degree in Life Sciences, Health Informatics, or a related field.
• Minimum of 7 years of experience in clinical data management within the pharmaceutical industry.
• In-depth knowledge of EDC systems (e.g., Medidata Rave, Oracle Clinical).
• Strong understanding of GCP, ICH guidelines, and CDISC standards.
• Proven experience in managing multiple clinical trials simultaneously.
• Excellent attention to detail and organizational skills.
• Strong leadership and communication abilities.
• Ability to work independently and as part of a remote team.

This is an exceptional opportunity to make a significant impact in the pharmaceutical sector from a remote location.

Our client is seeking a meticulous and experienced Remote Clinical Data Manager to play a vital role in their oncology research programs. This fully remote position allows you to contribute significantly to groundbreaking clinical trials from the comfort of your own home, with a primary focus on the **Nottingham, Nottinghamshire, UK** region's patient data but managed globally. You will be responsible for the end-to-end management of clinical trial data, ensuring its accuracy, completeness, and compliance with regulatory standards (e.g., ICH-GCP, FDA). Key responsibilities include developing data management plans, designing electronic data capture (EDC) systems, setting up edit checks, managing data review processes, and overseeing database lock.

The ideal candidate will possess a Bachelor's or Master's degree in a relevant life science or health-related field, coupled with a minimum of 3-5 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry, specifically in oncology. Proficiency with EDC systems (e.g., Medidata Rave, Oracle Clinical) and a strong understanding of clinical trial processes are essential. You must be highly organised, detail-oriented, and capable of managing multiple projects simultaneously in a remote setting. Excellent communication skills are required to liaise effectively with internal teams (clinical operations, biostatistics, programming) and external vendors. This role demands a proactive approach to problem-solving and a commitment to maintaining data integrity and patient confidentiality. You will be instrumental in ensuring the successful execution of clinical trials by providing high-quality data that supports critical decision-making.

Our client, a forward-thinking pharmaceutical research organization, is seeking an experienced Senior Clinical Data Manager to join their global team on a fully remote basis. This vital position will play a key role in ensuring the accuracy, integrity, and completeness of clinical trial data, which is fundamental to the success of our drug development programs. The ideal candidate will have a robust understanding of clinical trial processes, data management principles, and relevant regulatory requirements (e.g., FDA, EMA). You will be responsible for developing data management plans, overseeing database design and validation, managing data cleaning activities, and ensuring timely database lock. This role is perfectly suited for a seasoned data professional who is highly organized, detail-oriented, and proficient in managing complex projects in a remote work environment.

Key Responsibilities:

• Develop and implement comprehensive Clinical Data Management Plans (CDMPs).
• Oversee the design, build, and validation of clinical databases using EDC systems.
• Develop data validation specifications and perform data review and cleaning activities.
• Manage query generation, resolution, and tracking to ensure data accuracy.
• Lead the process for database lock, ensuring all data is complete and validated.
• Ensure compliance with relevant regulatory guidelines (e.g., GCP, ICH, CDISC) and company SOPs.
• Liaise with clinical operations, biostatistics, and programming teams to ensure seamless data flow.
• Provide technical expertise and guidance to junior data managers and study team members.
• Contribute to the development and maintenance of data management tools and processes.
• Manage outsourced data management activities with CROs, as applicable.

This role is entirely remote, requiring strong analytical skills, excellent communication abilities, and a proven track record of working effectively in a distributed team. The successful candidate will be adept at utilizing electronic data capture (EDC) systems and other data management software. You will be instrumental in upholding the quality and integrity of clinical data that supports critical regulatory submissions and product approvals. This is an outstanding opportunity to advance your career in clinical data management with a leading pharmaceutical company that values innovation and collaboration, all while working remotely from Birmingham, West Midlands, UK .
The ideal candidate will possess a Bachelor's degree in a relevant scientific discipline (e.g., Health Informatics, Statistics, Computer Science) or equivalent experience. A minimum of 7 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry is required, with at least 2 years in a lead or senior role. Expertise with major EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC) is essential. Proficiency in CDISC standards (SDTM, ADaM) is highly desirable. Strong understanding of GCP and regulatory requirements for clinical trials is mandatory. Excellent problem-solving, organizational, and project management skills are necessary. The ability to work independently, manage multiple studies concurrently, and meet tight deadlines in a remote environment is crucial. Exceptional communication skills, both written and verbal, are needed to collaborate effectively with global teams.

Our client, a leading international contract research organization (CRO) specializing in oncology, is seeking a meticulous and experienced Remote Clinical Data Manager to support their groundbreaking clinical trials. This is a fully remote position, offering the opportunity to contribute to life-saving research from anywhere. You will be responsible for ensuring the quality, integrity, and completeness of clinical trial data collected from various sites globally. Your role involves database design and setup, data review and cleaning, query management, and ensuring compliance with regulatory standards (e.g., GCP, CDISC).

As a remote team member, you will collaborate closely with clinical research associates (CRAs), biostatisticians, and study physicians in a virtual setting. Excellent communication and organizational skills are crucial for effective remote teamwork. You will be proficient in clinical data management software and possess a strong understanding of clinical trial processes. The ideal candidate will have a keen eye for detail, a systematic approach to data handling, and a commitment to upholding the highest standards of data accuracy and regulatory compliance. Experience in oncology trials is highly desirable.

Key Responsibilities:

• Oversee the end-to-end clinical data management process for oncology studies.
• Design, build, and validate clinical databases (e.g., EDC systems) in accordance with study protocols and standards.
• Develop data management plans (DMPs) and data review guidelines.
• Execute data validation checks, identify data discrepancies, and generate/resolve data queries.
• Perform SAE reconciliation and ensure timely reporting of serious adverse events.
• Collaborate with clinical operations and medical teams to ensure data accuracy and completeness.
• Manage database lock processes and ensure data integrity for statistical analysis.
• Contribute to the development and maintenance of data management SOPs.
• Ensure compliance with ICH-GCP guidelines and other relevant regulatory requirements.
• Train and mentor junior data management staff as needed.

Qualifications:

• Bachelor's degree in Life Sciences, Health Information Management, or a related field.
• Minimum of 5 years of experience as a Clinical Data Manager in pharmaceutical or CRO settings.
• Extensive experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical).
• Strong understanding of CDISC standards (SDTM, ADaM) is essential.
• Experience managing oncology clinical trials is highly preferred.
• Proficiency in data analysis and reporting tools.
• Excellent understanding of ICH-GCP and other relevant regulatory guidelines.
• Exceptional attention to detail and organizational skills.
• Strong written and verbal communication skills for effective remote collaboration.
• Ability to work independently and manage multiple priorities in a remote setting.

This fully remote role, supporting our client's extensive research activities originating from their UK operations, particularly concerning studies linked to Newcastle upon Tyne, Tyne and Wear, UK , offers a competitive compensation package and the opportunity to make a significant impact in oncology clinical research.

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

We're Hiring: Clinical Nurse

Focus Area: Multiple Myeloma Research

Are you a Band 6 Nurse with a keen eye for detail and a passion for clinical research? We're looking for someone to join our team at Milton Keynes University Hospital on a part-time basis (2–3 days/week) to support a research study in Multiple Myeloma .

What you'll be doing:

• Patient identification and recruitment
• Accurate clinical data entry
• Supporting research operations on-site

What we're looking for:

• NMC-registered Band 6 Nurse
• Experience with patient identification and clinical data entry
• Availability on Wednesdays , plus two additional weekdays
• Strong communication and organisational skills
• This is a great opportunity to contribute to impactful research while maintaining a flexible schedule.