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Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

Systems Test Engineer – Digital Health + MedTech + Healthcare Sector Location: Oxford (on-site 90%, with occasional remote flexibility) Are you someone who enjoys understanding how systems work and making sure they work reliably? Do you find satisfaction in digging into data, spotting inconsistencies, and helping technology perform at its best? Looking for a hands-on role that brings together devices, software, and meaningful outcomes? This might be the opportunity you’ve been looking for. The Opportunity We’re supporting a growing organisation working quietly at the intersection of health, data, and engineering. Their platform is already deployed in research settings worldwide, capturing vital information through smart, non-invasive systems. As a Systems Test Engineer, you will ensure that this complex and high-impact platform runs as it should. That means digging into both hardware and software, developing practical testing approaches, and validating data accuracy to a high standard. You'll also work closely with a supportive team of engineers and scientists who value thoughtful problem-solving. Why This Role Stands Out • Take ownership of testing across integrated systems including hardware, software, and data, • Help shape how the team approaches test automation, defect management, and quality processes, • Contribute to validation efforts that benchmark product performance against clinical standards, • Gain exposure to a unique combination of IoT hardware and cloud-based tools, • Be part of a thoughtful and mission-driven team in a hands-on setting What You’ll Bring (or Be Keen to Build On) You’re probably from a technical background and enjoy working with systems that combine physical devices and software. You may have tested similar integrated products before, or you might bring experience from QA, support engineering, or early product development. Skills and experience that would be useful: • Designing and running system-level tests, • Managing bugs and contributing to the full development lifecycle, • Working in quality-sensitive or regulated environments, • Using Python or other scripting tools to automate or streamline checks, • Understanding how to validate data as well as functionality But this isn’t a box-ticking exercise. If you’re excited by how complex systems work and enjoy problem-solving, we’d love to hear from you. A Bit About the Team This is an on-site role based in Oxford, with flexibility for occasional remote working. You’ll be working closely with a team that values care and rigour in what they build. There is a good balance between structure and flexibility, with a shared focus on doing high-quality work in a practical, friendly environment. What’s on Offer • A competitive salary that reflects your expertise, • Opportunities to learn and grow across software, hardware, and data systems, • Involvement in projects that contribute to clinical and research outcomes, • Exposure to emerging technologies in real-world settings, • A supportive and collaborative team culture How to Apply If you're looking to apply your skills in a setting where quality really matters, and where your work connects directly to people and outcomes, we’d love to hear from you. Inclusion Matters We’re committed to inclusive recruitment practices. If you're not sure you meet every point listed, please get in touch anyway. We’re interested in potential, not perfection.

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

Physiomics Physiomics plc (AIM: PYC) is an Oxford-based contract research organisation and consultancy specialising in the application of mathematical and data science solutions to support the development of therapeutic drugs and personalised medicine dosing software. Physiomics has a current turnover of circa £1m p.a. It has a high-profile brand and an established customer base of clients in the UK, Europe and North America. Physiomics takes a collaborative approach to provide clients with bespoke solutions encompassing data, analytics and insight. Physiomics is structured in two service-lines; Model Informed Drug Development (MIDD) and Biometrics. The Company’s MIDD service-line provides a full range of pharmacokinetic/ pharmacodynamic contract services to companies ranging from biotechs to some of the largest pharmaceutical companies in the world, across multiple therapeutic areas. The Company uses a range of commercially available software solutions but also maintains its own proprietary Virtual Tumour™ model which simulates the effects of anti-cancer agents on pre-clinical and human tumours, helping clients to improve the success rate of drug discovery and development projects while reducing time and cost. The MIDD service-line has completed over 140 commercial projects, involving over 125 targets and drugs, and has worked with clients such as Merck KGaA, Numab Therapeutics, Cancer Research UK and Bicycle Therapeutics, to name but a few. The Company recently expanded its contract services into the field of Biometrics, which is run as a separate service-line and provides biostatistics, statistical programming and data management solutions. Even though only recently launched, this service-line is already delivering on several client contracts and has a rapidly growing pipeline of opportunities being progressed. Separately from its contract services business, Physiomics has won several Innovate UK and NIHR grants which it has used to develop a software tool to personalise the dose of chemotherapy. It has an ongoing collaboration with US company, DoseMe, and has incorporated this tool into their existing commercial platform (DoseMeRx). The dosing software tool is currently available for research use only, but as the tool is further developed, the plan is to implement paid for functionality. The CEO Role Physiomics is seeking a new leader to drive an ambitious program of expansion and strategic change within an LSE AIM-listed business. The role requires excellent influencing skills, keen commercial acumen and the ability to communicate effectively with both scientific/ clinical and commercial stakeholders. Even though prior experience is not necessary, the role will be responsible for managing all corporate activities pertaining to being a public company, work with the board of directors, Company Secretary, NOMAD and Broker to ensure compliance to AIM rules and effective governance of the business. Physiomics’ revenues are derived mostly from its core contract services business, and this will remain the first priority of the incoming CEO who will be able to support the acquisition and retention of clients, participate in key meetings and presentations, lead the internal team and have the experience and gravitas to act as a senior advisor to key client contacts. The Company currently operates virtually, although the CEO will need to be available for regular face to face team meetings in the Oxford / London area. The role will require occasional travel (in the UK and abroad) to clients, networking activities, and meetings with stakeholders. The company currently has 12 permanent employees (including Board Directors) and utilises contractors to provide additional capacity and expertise when required. The Company operates a fee for service revenue model but has developed a personalised dosing tool that could form the basis of a software-as-a-service offering. Physiomics believes this role represents a real opportunity for the right individual to make a significant impact in a small organisation. Key responsibilities of the role Operational • Set the Company’s overall strategy, balancing core consulting with other activities such as personalised medicine, • Accountable for all business development and marketing activities (BDM), supporting the Head of Business Development and heads of service-lines (MIDD and Biometrics) to develop and execute on an effective BDM strategy to identify and win new business, maximise pipeline size and quality, and further grow the Physiomics brand., • Accountable for the delivery and expansion of high-quality consultancy services, supporting heads of service-lines in effective resource management to achieve excellence in consulting and develop new service capabilities aligned with growth objectives., • Accountable for general business operations, including HR and recruitment, quality, IT, business processes and management of key internal initiatives., • As required, support key client engagements, providing strategic scientific/ clinical input (depending on experience) to key projects, to ensure client satisfaction and maximise repeat business, • Ensure robust and timely management reporting and communication, including for monthly board meetings, • Liaise with NOMAD, legal advisors and the Company’s broker to ensure compliance with AIM, MAR, QCA and other applicable regulations and guidelines, • Maintain corporate policies and procedures in support of applicable corporate governance and employment regulations (e.g. share trading, GDPR, social media, anti-bribery etc), • Be responsible (together with NOMAD and broker) for the timely issuance of press releases via LSE’s Regulatory News Service where required, • Develop and communicate interim (half year) and full year annual reports to shareholders, • Set up and run the Company’s Annual General Meeting, • Set appropriate remuneration for employees, directors and officers through the Company’s board and remuneration sub-committee, including (as appropriate) bonuses and share options Candidate profile The successful candidate will be an experienced, high calibre international business executive, with an entrepreneurial spirit and evidence of driving successful growth and innovation. They are likely to have experience in delivering contract services (either as an individual or as part of a larger organisation) and a good knowledge of life sciences (for example drug development or technologies used in support of pharmaceutical R&D or clinical practice). They will be motivated to work in a small company environment where they can make a significant impact. Professional/technical experience • A proven track record of success in growing small/ medium sized service businesses or business units in life-sciences, preferably in biopharma R&D, • Extensive current client contacts across the biotech and pharmaceutical industry sector., • Prior experience of running a company or leading a team of scientific professionals within either a CRO or biopharma setting., • An understanding of the R&D process for therapeutic drug development and its challenges, • Knowledge of the international pharmaceuticals and biotechnology sector, • Strong interest in experience of working in a small company environment; willingness to roll up sleeves and get involved in a wide variety of activities, • Experience or knowledge of issues connected with running a public company helpful but not essential, • Hands-on experience in one or more of the following areas: quantitative pharmacology, clinical pharmacology, biometrics and clinical development is desirable. Qualifications • Good scientific or clinical credentials, ideally to PhD/ MD level, • Demonstrated financial acumen either through relevant experience or a qualification such as MBA Personal attributes • Self-motivated, with a readiness to take on tough challenges and see them through to conclusion, • Results focussed: Ability to set a strategic agenda and to execute to achieve long-term growth, • Good business acumen: Good understanding of the services business model and the factors to manage for successful growth, • Excellent communication skills; able to present arguments in a diplomatic, clear, concise, and logical manner, and to influence others positively, • Confidence, persona and gravitas to interface and negotiate with senior client contacts, and to confidently sell the Company’s capabilities to the outside world, • Demonstrated ability to resolve problems in a creative and positive manner and effectively maneuver through complex situations – internal and external, • A strong team leader with the flexibility to work with a wide range of skillsets and personalities consisting of the internal team, consultants, clients and third parties

Metric Bio is partnering with a rapidly growing, mission-driven medical technology company to recruit a Digital Architect for a critical on-site role in Oxford. This is a senior, blended position combining hands-on technical architecture with technical leadership and delivery ownership. You’ll act as the primary technical authority across internal engineering teams and an external delivery partner, playing a central role in shaping and executing the company’s digital strategy. The organisation has an ambitious digital roadmap for the coming year, focused on evolving and scaling core platforms in a regulated environment. A significant focus of the role will be ensuring platforms are scalable, compliant, and submission-ready for regulatory approval, while also maturing engineering practices and architectural governance. Key responsibilities include: • Owning end-to-end digital architecture across cloud, applications, IoT, and data platforms, • Leading architectural decision-making and guiding hands-on implementation, • Managing and improving delivery with an onshore/offshore external development partner, • Providing technical leadership to a small internal engineering team, • Ensuring systems meet regulatory, security, and safety-critical standards, • Supporting greenfield initiatives alongside live clinical platforms Key experience sought: • Proven experience in a Digital Architect or senior technical leadership role, • Strong background across cloud (Azure preferred), applications, APIs, and IoT-enabled systems, • Experience working in regulated or safety-critical environments (digital health, medical devices, fintech, automotive, rail, etc.), • Ability to balance technical depth with business-led decision-making, • Comfortable working fully on-site in Oxford This is an excellent opportunity to step into a highly visible role with real-world impact, shaping digital platforms that directly affect patient outcomes.

Metric Bio is working with an innovative medical technology organisation seeking a Senior Full Stack Developer to join their on-site engineering team in Oxford. This is a hands-on role suited to an experienced engineer who enjoys working across the full stack in a safety-critical environment. You’ll contribute to both clinical and messaging platforms, working closely with internal stakeholders and external partners to deliver high-quality, scalable digital solutions. The technology environment is predominantly Microsoft/Azure-based, with modern front-end frameworks and a strong focus on connected devices and data-intensive systems. Key responsibilities include: • Building and maintaining web and application platforms using React and modern JavaScript frameworks, • Developing and supporting backend services, APIs, and integrations within an Azure environment, • Contributing to messaging and clinical applications, including future platform evolution, • Working with IoT-generated data, including time-series and event-based streams, • Supporting engineering best practices in a regulated, safety-critical context Key experience sought: • Strong full stack development experience, • React experience essential; experience with .NET, SQL, and Azure highly desirable, • Exposure to cloud services, APIs, and data-driven systems, • Experience in regulated or safety-critical domains (medical devices, fintech, defence, rail, automotive, etc.), • A mature engineering mindset with a strong understanding of quality, standards, and world class engineering looks like. This role offers the chance to work on meaningful technology in a collaborative on-site environment, with long-term product ownership rather than consultancy-style delivery.

As a Clinical Business Intelligence Manager, you will lead the design and delivery of analytics that connect clinical, operational, and performance data to real‑world healthcare decisions. Position: Clinical Business Intelligence Manager. Lead and mentor a business intelligence team in building da

Data Analytics, Microsoft Access, SQL, Power BI, R, Data Visualization, Tableau, Data Management, Data Mining, SAS, Data Analysis Skills, Analytics. Support clinical studies including CRF design/review database build and validation creation of data management documents. In this role you would be joi

This is an exciting opportunity to undertake a one-year clinical fellowship, designed to provide sub-specialty experience in pulmonary intervention.

A leading biopharma company is seeking a Clinical Trials Specialist Apprentice to support the planning and delivery of clinical trials. The role involves assisting with setup, data management, documentation, and site coordination.

A leading global healthcare consulting firm in the United Kingdom is seeking an experienced Senior Data Management Programmer. The role involves leading programming tasks for clinical trials while owning specifications and validation processes. Candidates should have 5+ years of SAS programming expe

A full-service clinical contract research organization in Greater London is seeking an experienced informaticist to lead advanced analyses and create predictive data models.

The role involves coding medical information, supporting clinical staff, and ensuring accurate data entry into the organization's systems.

The post holder will be required to accurately enter large amounts of research and patient data and to ensure that the data are stored appropriately according to the data protection act and in line with the ethical approval for the projects involved. Accurately and efficiently enter patient data on

A leading global university in the UK seeks a Senior Data Manager for the Birmingham Clinical Trials Unit. The role involves managing clinical research data, ensuring accuracy, and providing support to multi-disciplinary research groups. Candidates should have a degree in a biomedical field and expe

A leading medical laboratory hub in the UK is seeking a candidate for a role focused on medical coding and administration of clinical data. The responsibilities include ensuring data security, summarizing medical information, managing risk in practices, and mentoring junior staff.

A leading global biopharmaceutical solutions organization is seeking a Sr Clinical Data Scientist to lead the coordination of data collection for clinical studies. Candidates should have experience with Veeva Vault and a strong background in clinical data management. This role involves ensuring data

The successful candidate will conduct and present detailed analyses of clinical and health data and collaborate closely with Statisticians.

A leading AI technology firm is seeking a Principal Clinical Scientist to drive expertise in clinical trial design and ensure regulatory standards in data interpretation. The ideal candidate will possess senior-level experience in clinical trials, a strong background in research methodology, and the

A leading clinical research organization is seeking a Senior Data Scientist to lead advanced analyses and develop predictive models to inform clinical study designs. This role contributes to team growth and supports data-driven decisions, impacting patient outcomes in the pharmaceutical sector.

A health service provider in the North East UK seeks a Senior Administrator / Clinical Coder to ensure accurate clinical data entry and promote effective use of health information.

A leading healthcare company in the UK is seeking a Lead Data Scientist to design and develop LLM-based solutions that accelerate drug development and improve patient care.

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 be the escalation point and poi

A leading research institution in Greater London seeks an experienced Clinical Trial Manager to oversee the trial management of an innovative project aimed at tackling antimicrobial resistance.

A leading NHS Trust in Greater London is seeking a Clinical Informatics Specialist to enhance clinical practices through data analysis and user-friendly tools. This role involves supporting the Clinical Informatics Service via project implementation and sustainability efforts. Ideal candidates shoul

Proclinical is seeking a Clinical Data Manager to join a dynamic team focused on improving patient outcomes in cardiothoracic surgery. In this role, you will play a key part in enhancing database onboarding, data curation, and ensuring data quality. Knowledge of international data standards and comm

A prominent pharmaceutical company in Hertfordshire is looking for a Clinical Database Programmer to support the transition to electronic data capture. The role involves building and maintaining study databases, ensuring data quality, and managing data integration with external vendors. Candidates s

Key performance indicators dictated by Healthcare for London and patient outcomes are monitored and assessed regularly, and an active programme of internal audit within the stroke service provides essential data for clinical governance purposes. Standard Operating Procedures (SOPs) for major element

A leading health tech company in the UK is seeking a Senior UX Designer to shape data-driven, AI-enabled experiences in clinical trials.

Key responsibilities include ensuring high standards of data collection, managing trial documentation, and supporting the clinical research team. A leading cancer research facility is seeking a Clinical Trials Administrator to support paediatric cancer research. This role does not involve patient co

A leading clinical research organization in the United Kingdom is seeking a Data Manager to oversee and coordinate data management activities in clinical projects. Successful candidates will have experience in data management, strong communication skills, and an understanding of clinical trial proce

A leading healthcare company is seeking a Principal Clinical Data Management Analyst to join their Data Management team in Witney. This leadership role involves overseeing clinical data management activities and supporting R&D projects.

Acts as central steward of clinical data quality, monitors risks through the holistic review of clinical and operational data, using high level knowledge of the protocol, taking into account the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross f

A leading life science consulting firm in the United Kingdom is looking for a Data Manager to oversee the data management strategy for various projects. The ideal candidate will have a Bachelor's degree in Mathematics and experience in clinical trials. Responsibilities include developing metrics rep

This full-time position involves maintaining data management systems, liaising with collaborators, and ensuring accuracy through data entry.

A healthcare consulting firm is seeking a Lead CDM responsible for the end-to-end delivery of data management services for disease registry studies. This remote position requires significant experience, specifically over 7 years in data management and at least 4 years in budget management and client

Responsibilities include coding clinical correspondence, processing safeguarding documentation, and assisting in the COVID pandemic response.

Support clinical studies, including CRF design/review, database build and validation, creation of data management documents. In this role, you would be joining a vibrant, friendly and inclusive group of Data Managers, EDC programmers and Statistical Programmers, where you can expect to work across a

This role focuses on providing technical support for clinical documentation projects, developing training programs, and optimizing processes. Ideal candidates will have strong technical expertise and a background in clinical documentation.

We are hiring a Clinical Data Manager/Senior Clinical Data Manager based in the UK.

A healthcare organization based in Greater London is looking for a Divisional Research Nurse to support a diverse portfolio of clinical research studies including neurological conditions. Essential qualifications include being a Registered Nurse, along with relevant experience in clinical trials.

We are hiring a Senior Data Scientist (Clinical Data Analytics) to play a central role in the analysis and interpretation of clinical data collected from in‑vivo testing of our device. Senior Data Scientist (Clinical Data Analytics). You will work closely with the clinical team to support trial de

Have knowledge of database structure and data management techniques,. Experience in clinical trials in a comparable capacity. Demonstrated ability to oversee the autonomous completion of several projects or programs using comprehensive data management research life cycles.

The ideal candidate will hold a relevant degree and have experience in clinical research and a strong understanding of eCOA.

A leading health technology company in Witney is seeking a Principal Clinical Data Management Analyst to provide team leadership and clinical data management expertise for Clinical Affairs and R&D. The role involves managing data management activities across clinical studies and R&D projects and dev

Strong knowledge of clinical data management processes and regulatory requirements (GCP). The Lead CDM is responsible for the end-to-end delivery of data management services for disease registry studies. This role serves as the primary point of contact for data management on assigned projects, ensur

A leading biopharmaceutical company is seeking a Senior Manager, Data Management to lead clinical studies and oversee data management activities. Ideal candidates will have over 6 years of experience in clinical data management, strong project management skills, and the ability to lead team initiati

A leading biostatistics firm is seeking an experienced professional to provide technical leadership in SAS programs for analyzing clinical trial data.