11 of 11 Electronic Patient Records Jobs in Reading

limited to typical and novel data collected through central labs and ECG, medical imaging, biomarker and genomics analysis, real world data sources, Electronic Health records, electronic patient reported outcomes, wearables and sensors and other digital data … clinical study setting. Experience developing data transfer agreements. E xperience working with novel external data e.g., Real world data, digital health technologies, Electronic Health records (HL7, FIHR) or similar. Advanced Level - see base level + relevant modifications below: Minimum of 5 years … Biomarkers, Genomics, imaging or similar. Demonstrated project management skills. Experience working with novel external data e.g., Real world data, digital health technologies, Electronic Health records (HL7, FIHR) or similar. This role is not eligible for UK visa sponsorship IQVIA is a leading More ❯

with: We are seeking an experienced IT Project Manager with hands-on expertise in RiO Electronic Patient Record (EPR) systems and a proven track record of managing system migrations within the NHS. This is a critical role within our digital transformation programme, focused on More ❯

and cloud infrastructure to support the delivery and management of a next-generation SaaS-based Electronic Patient Record (EPR) system for the NHS. Join our client in ensuring secure, scalable, and highly available deployments that support healthcare services 24 / 7. Key Requirements More ❯

Strong communication skills and demonstrated ability to engage with business stakeholders and product teams. Experience in data modeling , data warehousing (e.g., Snowflake , AWS Glue , EMR , Apache Spark ), and working with data pipelines . Leadership experience—whether technical mentorship, team leadership, or managing critical projects. Familiarity with Infrastructure as Code (IaC More ❯

data to insight, within the portfolio across several offerings including, Privacy Analytics, Patient Data Platforms, Patient data licensing (EMR & Claims), IQVIA NLP and OMOP ODHSI Responsibilities Achieve individual annual sales target based on selling to Pharmaceutical clients across the offering suite to attain TCV … player Why Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In RWS, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in … 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 https: / / jobs.iqvia.com IQVIA is a leading global provider of clinical More ❯

Flatiron Health data required . Essential Functions Lead development of statistical programs and conduct analyses using secondary real world data sources, including claims, EHR, HEOR, and genomic data. Support development of other study documents including protocols, analysis specifications, and study reports Lead the feasibility of real-world data sources … to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives. Plan and program the integration of data from multiple sources. Conduct analyses to characterize patient cohorts and QC datasets within time, budget, and quality … 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 https: / / jobs.iqvia.com IQVIA is a leading global provider of clinical More ❯

Flatiron Health data required . Essential Functions Lead development of statistical programs and conduct analyses using secondary real world data sources, including claims, EHR, HEOR, and genomic data. Support development of other study documents including protocols, analysis specifications, and study reports Lead the feasibility of real-world data sources … to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives. Plan and program the integration of data from multiple sources. Conduct analyses to characterize patient cohorts and QC datasets within time, budget, and quality … 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 https: / / jobs.iqvia.com IQVIA is a leading global provider of clinical More ❯

Flatiron Health data required . Essential Functions Lead development of statistical programs and conduct analyses using secondary real world data sources, including claims, EHR, HEOR, and genomic data. Support development of other study documents including protocols, analysis specifications, and study reports Lead the feasibility of real-world data sources … to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives. Plan and program the integration of data from multiple sources. Conduct analyses to characterize patient cohorts and QC datasets within time, budget, and quality … 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 More ❯

managing Corporate Responsibility / Sustainability compliance needs, including compliance with existing, emerging and new sustainability legislation, covering the areas of extended producer responsibility (EPR) and product sustainability. They will focus primarily on the EMEA region, expanding to a global scope as EPR and product sustainability needs expand geographically. They … requirements associated with regional and country level regulations can be met to ensure market access. This role will oversee the administration and execution of EPR (extended producer responsibility): Packaging, WEEE, Batteries, and other country level sustainability reporting needs such as energy / carbon reporting requirements. This person will support … relevant legislation globally and participate in impact assessment with relevant functions. Work with EHSS Chemical Governance staff where there is crossover between chemical and EPR legislation. Participate in all relevant Medtech Europe Groups covering forthcoming EPR, Packaging, Circular Economy and EcoDesign legislation. Work with other CEHSS team members and other More ❯

Client Summary: Innovative technology is transforming how hospitals and research sites transfer data for clinical trials. Seamless integration allows fast and accurate patient data transfer between systems. Significantly reduces the need for manual data transcription. Minimizes the requirements for source data verification (SDV … . Enhances efficiency, speed, and accuracy in clinical trial data collection processes. Position Responsibilities: Serve as a subject matter expert in the rapidly evolving EHR-to-EDC space, engaging, educating, and building partnerships with thought leaders and key stakeholders. Represent the organization with clients, embodying a vision for transformational change … technology to improve clinical trial delivery. At least 3 years of direct experience in, and competent technical knowledge of, clinical research software such as EHR / EDC / ePRO, or similar services used by clinical operations within pharmaceutical companies. Successful track record in business development and selling to More ❯

s technology solution that go on to deliver the expected benefits. Plan and execute the technical deployment and integration of Metadvice-AI with Practice EHR systems. Partner with practice and third-party staff to configure and test Metadvice prior to Clinical use. Monitor and report on project progress, identify issues … and development of training materials and UK and EU regulated documents relating to installation, use and training Documentation and Contract Management: Maintain accurate records of all client interactions, approvals, and project-related documentation. Ensure all required contracts are signed and in place. Act as our CRM (SalesForce More ❯