622 Clinical Data Manager jobs in the United Kingdom

This is a fully remote opportunity for a skilled Clinical Data Manager to join a leading global pharmaceutical research organization. Our client is at the forefront of developing life-changing therapies and seeks a dedicated professional to manage and oversee clinical trial data from study start-up through database lock. You will be responsible for developing Data Management Plans (DMPs), designing Case Report Forms (CRFs), and establishing data validation checks and edit specifications in accordance with protocol requirements and regulatory guidelines (e.g., ICH GCP). This role involves leading data cleaning activities, ensuring the accuracy, completeness, and integrity of clinical trial data. You will collaborate closely with biostatisticians, clinical research associates (CRAs), study managers, and external vendors to resolve data discrepancies and queries in a timely manner. Database validation and User Acceptance Testing (UAT) will be key responsibilities, ensuring the clinical database meets all functional and data integrity requirements. You will also contribute to the development and maintenance of data management SOPs and work instructions. A strong understanding of CDISC standards (SDTM and ADaM) and EDC systems (e.g., Medidata Rave, Oracle InForm) is essential. Experience in managing data for Phase I-IV clinical trials across various therapeutic areas is highly desirable. The ideal candidate will possess a Bachelor's degree in a scientific discipline, computer science, or a related field, with a minimum of 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry. Exceptional attention to detail, strong organizational skills, and the ability to manage multiple projects simultaneously are crucial. Excellent communication and interpersonal skills are necessary for effective remote collaboration. This is a remote-first position, offering the flexibility to work from anywhere within the UK, with regular virtual team meetings and collaboration. If you are a proactive and experienced Clinical Data Manager looking for a challenging and rewarding remote role, we encourage you to apply.

Our client, a rapidly growing global Contract Research Organisation (CRO), is seeking an experienced and highly motivated Lead Clinical Data Manager to join their dynamic team. This is a fully remote position, allowing you to work from any location within the UK. You will be responsible for overseeing the management of clinical trial data from study start-up through database lock and close-out. This includes leading data management activities, ensuring data quality, integrity, and compliance with regulatory requirements (e.g., GCP, ICH). Your responsibilities will encompass database design and development, data validation planning and execution, query management, and user acceptance testing. You will lead a team of data managers, providing guidance, training, and mentorship. The ideal candidate will possess a strong understanding of clinical trial processes, EDC systems, and data standards (e.g., CDISC). You will have excellent analytical and problem-solving skills, with a meticulous attention to detail. Proven leadership experience and the ability to manage multiple projects concurrently in a remote setting are crucial. We are looking for a proactive individual with exceptional communication and interpersonal skills, capable of effectively collaborating with cross-functional teams, including clinical operations, biostatistics, and medical writing. This role offers a competitive salary, a comprehensive benefits package, and the opportunity to work on diverse and impactful clinical research projects within a supportive and collaborative remote-first culture. You will play a critical role in ensuring the accuracy and reliability of data that underpins critical medical research.

Our client, a rapidly expanding pharmaceutical research organization, is seeking an exceptional Principal Clinical Data Manager to spearhead their data management initiatives. This fully remote position offers a unique chance to influence the strategic direction of clinical data operations, working with groundbreaking therapeutic areas and contributing to life-saving drug development. You will be instrumental in ensuring the integrity, accuracy, and completeness of clinical trial data, adhering to the highest industry standards and regulatory requirements.

As a Principal Clinical Data Manager, you will lead the design, development, and implementation of robust clinical data management systems and processes. Your responsibilities will include developing Data Management Plans (DMPs), creating Case Report Forms (CRFs), establishing data validation checks, and managing database builds and transfers. You will oversee the entire data lifecycle, from data collection and cleaning to database lock and archiving. Furthermore, you will play a crucial role in mentoring and guiding junior data managers, fostering a culture of excellence and continuous improvement. Collaboration with cross-functional teams, including biostatisticians, clinical scientists, and regulatory affairs, will be essential to ensure seamless project execution. The ability to anticipate potential data issues and proactively implement solutions will be key to your success.

The ideal candidate will possess a Bachelor's or Master's degree in a scientific or related discipline, complemented by a minimum of 8 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry. A proven track record of managing complex, multi-center clinical trials, including experience with various Electronic Data Capture (EDC) systems, is mandatory. You should have a deep understanding of Good Clinical Practice (GCP), FDA regulations, and other relevant global regulatory guidelines. Exceptional analytical, problem-solving, and project management skills are required. Strong leadership capabilities, excellent communication and presentation skills, and the ability to thrive in a fast-paced, remote environment are essential. This role demands a strategic thinker who can not only execute but also innovate and elevate our client's data management capabilities. Experience with specific therapeutic areas, such as oncology or infectious diseases, would be a significant advantage.

Key Responsibilities:

• Lead the development and implementation of clinical data management strategies.
• Oversee the design, UAT, and implementation of EDC systems.
• Develop and maintain Data Management Plans (DMPs) and other critical documentation.
• Ensure data quality, integrity, and compliance with regulatory standards (GCP, ICH).
• Manage data review, cleaning, and reconciliation activities.
• Facilitate database lock and archival processes.
• Provide technical expertise and guidance to data management teams.
• Collaborate with study teams to ensure timely and accurate data delivery.
• Contribute to process improvements and SOP development.
• Mentor and train junior data management personnel.

Required Qualifications:

• Bachelor's or Master's degree in a scientific field.
• 8+ years of experience in clinical data management in pharma/biotech.
• Extensive experience with EDC systems (e.g., Medidata Rave, Oracle Clinical).
• In-depth knowledge of GCP, ICH, and FDA/EMA regulations.
• Proven leadership and team management skills.
• Excellent analytical and problem-solving abilities.
• Strong communication and interpersonal skills.
• Ability to work independently and manage multiple projects remotely.

This is an exciting opportunity to join a company at the forefront of medical innovation, offering the flexibility of a fully remote role. If you are ready to take on a leadership challenge and make a significant contribution to pharmaceutical research, apply today for this role based near Belfast, Northern Ireland, UK .

Our client, a leading biopharmaceutical company dedicated to advancing patient care through innovative therapies, is seeking a Principal Clinical Data Manager for their facility in Brighton, East Sussex, UK . This critical role involves overseeing the design, development, and implementation of clinical databases for global clinical trials. You will be responsible for ensuring the accuracy, integrity, and quality of clinical trial data in compliance with regulatory requirements (e.g., FDA, EMA) and Good Clinical Practice (GCP) guidelines. This position requires extensive experience in clinical data management, including database design, data validation strategies, and data cleaning processes. You will lead a team of data managers, providing guidance, mentorship, and technical expertise. Key responsibilities include developing and maintaining Data Management Plans (DMPs), establishing data standards, and ensuring adherence to study protocols. You will collaborate closely with clinical operations, biostatistics, and clinical programming teams to ensure timely database lock and efficient data analysis. The Principal Clinical Data Manager will also be involved in vendor management, evaluating and overseeing third-party data management service providers. Experience with Electronic Data Capture (EDC) systems is essential, and proficiency in statistical analysis software is a plus. This role demands strong leadership skills, excellent communication abilities, and a meticulous attention to detail. You will play a pivotal role in ensuring the successful execution of clinical trials, contributing directly to the development of life-saving medications. The role offers a dynamic and challenging work environment with opportunities for professional growth and development. We are looking for an experienced professional who can drive data management excellence and contribute significantly to our mission of improving global health. The hybrid work model allows for a balanced approach, combining essential in-office collaboration with remote flexibility.

Our client is looking for a meticulous and experienced Remote Clinical Data Manager to join their innovative pharmaceutical team. This position is fully remote, offering flexibility and the opportunity to work from anywhere within the UK. You will be responsible for overseeing the collection, quality, and integrity of clinical trial data, ensuring compliance with regulatory standards (e.g., GCP, ICH). This role involves close collaboration with clinical operations, biostatistics, and programming teams to design data collection systems, develop data management plans, and manage database lock procedures.

Key responsibilities include developing clinical data management system (CDMS) specifications, creating electronic data capture (EDC) forms, and implementing data validation checks. You will also be responsible for querying data discrepancies, ensuring timely resolution, and performing quality control reviews of datasets. The Remote Clinical Data Manager will contribute to the development of standard operating procedures (SOPs) and work instructions related to data management. Furthermore, you will ensure that all data management activities are documented thoroughly and maintained in accordance with regulatory requirements.

The ideal candidate will possess a Bachelor's degree in a scientific or healthcare-related field, with a 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, Veeva Vault EDC) and a strong understanding of clinical trial processes and regulatory guidelines are essential. Excellent analytical, problem-solving, and organizational skills are required, along with strong attention to detail. The ability to work independently, manage multiple priorities effectively, and communicate clearly in a remote environment is crucial. This is an excellent opportunity for a skilled professional to make a significant impact in drug development while enjoying the benefits of a remote-first work culture.

Our client, a leading pharmaceutical research organisation, is seeking a highly skilled and meticulous Senior Clinical Data Manager to join their innovative global team. This is a critical, fully remote position requiring extensive experience in clinical data management within the pharmaceutical or biotech industry. You will be responsible for ensuring the quality, integrity, and accuracy of clinical trial data from study start-up through database lock and submission. The role involves leading data management activities, developing data management plans, performing data review and cleaning, and ensuring compliance with regulatory standards (e.g., GCP, ICH). As a remote-first role, you will collaborate extensively with study teams, clinical operations, biostatistics, and external vendors to achieve project milestones. This is an exceptional opportunity to contribute to life-saving research from the comfort of your home.

Key Responsibilities:

• Lead and manage clinical data management activities for assigned clinical trials.
• Develop and maintain Data Management Plans (DMPs) in collaboration with cross-functional study teams.
• Design, build, and validate clinical databases (e.g., EDC systems) and data collection tools.
• Oversee data entry, data validation, query generation, and data cleaning processes to ensure data accuracy and completeness.
• Perform data review and reconciliation activities, including SAE reconciliation and external data reconciliation.
• Ensure compliance with all applicable regulatory requirements (GCP, ICH, FDA, EMA) and company SOPs.
• Manage vendor activities related to data management, including EDC providers and central labs.
• Prepare and present data management status updates to project teams and management.
• Participate in the development and implementation of data management standards and best practices.
• Contribute to the validation of data management systems and tools.
• Support database lock activities and ensure the quality of the final clinical database.

Qualifications:

• Bachelor's degree in a scientific, medical, or computational field. Advanced degree preferred.
• Minimum of 7 years of experience in clinical data management in the pharmaceutical or biotech industry.
• Extensive experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle InForm, Veeva EDC).
• Thorough understanding of clinical trial processes, regulatory guidelines (GCP, ICH), and data standards (CDISC).
• Proven ability to manage complex clinical datasets and ensure data quality.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent communication, interpersonal, and organisational skills.
• Experience in developing DMPs, edit checks, and data validation plans.
• Ability to work independently, manage multiple projects, and meet tight deadlines in a remote environment.
• Proficiency in database management principles.

This role is crucial for our client's success and is based in Belfast, Northern Ireland, UK , though it is a fully remote position, offering maximum flexibility.

Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a highly skilled and experienced Senior Clinical Data Manager to join their dynamic team. This role, located in Wolverhampton, West Midlands, UK , operates on a hybrid model, offering a balance between collaborative office-based work and the flexibility of remote working. You will be responsible for ensuring the accuracy, integrity, and quality of clinical trial data, playing a pivotal role in the successful execution of drug development studies.

The Senior Clinical Data Manager will oversee all aspects of clinical data management, from database design and setup to data validation, query resolution, and database lock. You will lead data management activities for clinical trials, ensuring adherence to Good Clinical Practice (GCP), regulatory requirements (e.g., FDA, EMA), and company SOPs. This position requires a strong understanding of clinical trial processes, EDC systems, and data standards (e.g., CDISC). Your ability to manage complex datasets, mentor junior team members, and collaborate effectively with cross-functional teams will be critical to success.

Key Responsibilities:

• Lead the design, development, and UAT of clinical databases using EDC systems (e.g., Medidata Rave, Oracle Clinical).
• Develop data management plans (DMPs) and data validation plans (DVPs).
• Oversee the data cleaning process, including developing data review guidelines and resolving data queries.
• Perform quality control checks on data and ensure compliance with standards.
• Manage database lock activities in collaboration with project teams.
• Ensure compliance with ICH GCP guidelines, regulatory requirements, and company SOPs.
• Provide expertise and guidance on data management best practices.
• Train and mentor junior data management personnel.
• Liaise with clinical operations, biostatistics, and programming teams to ensure seamless data flow.
• Contribute to the development and implementation of data management tools and processes.

Qualifications and Experience:

• Bachelor's degree in a scientific, technical, or healthcare-related field.
• Minimum of 5 years of experience in clinical data management within the pharmaceutical or biotech industry.
• Extensive experience with Electronic Data Capture (EDC) systems.
• Thorough understanding of ICH GCP, CDISC standards (SDTM, ADaM), and regulatory requirements.
• Proven experience in database design, data validation, and query management.
• Excellent analytical, problem-solving, and organizational skills.
• Strong communication and interpersonal skills, with the ability to work effectively in a team.
• Ability to manage multiple projects simultaneously and meet strict deadlines.
• Experience with statistical analysis software is a plus.
• Relevant certifications (e.g., CDMP) are advantageous.

This is a challenging and rewarding opportunity for a dedicated Senior Clinical Data Manager to contribute significantly to life-saving pharmaceutical research.

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.
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Our client, a leading Contract Research Organisation (CRO) dedicated to advancing medical treatments, is actively seeking an experienced Senior Clinical Data Manager to join their growing, globally distributed team. This is a fully remote position, offering flexibility and the opportunity to contribute to critical clinical trials from the comfort of your own home. You will be responsible for overseeing the design, development, and execution of clinical databases, ensuring the integrity, accuracy, and quality of data collected during studies.

Key Responsibilities:

• Lead the design, database build, and validation of clinical databases according to study protocols and regulatory requirements (e.g., CDISC, ICH GCP).
• Develop Data Management Plans (DMPs) and contribute to other study-related documentation, such as CRFs, edit checks, and data validation plans.
• Oversee the data cleaning process, including query generation, resolution, and reconciliation, ensuring timely and accurate data review.
• Manage data entry and transfer activities, ensuring data integrity and compliance with SOPs.
• Coordinate with cross-functional teams, including clinical operations, biostatistics, programming, and medical monitors, to ensure efficient data flow and issue resolution.
• Provide guidance and mentorship to junior data managers and data management staff.
• Ensure adherence to all relevant regulatory guidelines and industry standards throughout the data management lifecycle.
• Participate in database validation activities, user acceptance testing (UAT), and system integration testing.
• Contribute to the development and implementation of data management standards, SOPs, and best practices.
• Manage multiple clinical studies simultaneously, ensuring all data management deliverables are met on time and within budget.
• Act as a key point of contact for data management aspects during client audits and regulatory inspections.
• Evaluate and implement new technologies and tools to enhance data management efficiency and quality.
• Contribute to the proposal process by providing input on data management timelines and resource requirements.
• Perform quality control checks on data management activities and deliverables.

Required Qualifications:

• Bachelor's degree in a life science, computer science, or related field. Master's degree preferred.
• A minimum of 5-7 years of experience in clinical data management within the pharmaceutical or CRO industry.
• Extensive experience with EDC (Electronic Data Capture) systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC).
• Strong understanding of clinical trial processes, data standards (CDISC), and regulatory requirements (ICH GCP, FDA).
• Proficiency in database design, data validation, and query management.
• Excellent leadership, communication, and interpersonal skills, with the ability to collaborate effectively in a remote team environment.
• Strong analytical and problem-solving abilities with meticulous attention to detail.
• Experience mentoring or supervising junior team members.
• Ability to manage multiple projects simultaneously and prioritize effectively.
• Proficiency in Microsoft Office Suite.
• Must be based in the UK and eligible to work remotely.

This is an excellent opportunity for a skilled professional to make a significant contribution to life-saving research in a flexible, remote working environment. Applicants must have the unrestricted right to work in the UK.