11 of 11 Electronic Patient Records Jobs in the South East

the Trust Executive Team, suppliers and in some cases, senior members of other organisations. This is a 'hands on' role that involves managing the development and configuration of electronic systems, availability management, change management and ensuring data integrity.The post holder will provide expert tier 3 support for critical application software used at the Trust and across the … monitoring of the Trust's Integration Engine (TIE) in order to support all interfacing activities which form the Trust's Electronic Patient Record (EPR). Working closely with Clinical and Administrative Subject Matter Experts to identify integration requirements throughout the lifecycle of Clinical Application Projects, from initiation to post go live. To constantly review … the Trust Executive Team, suppliers and in some cases, senior members of other organisations. This is a hands on role that involves managing the development and configuration of electronic systems, availability management, change management and ensuring data integrity. The post holder will also provide specialist escalated tier 3 support for relevant critical application software used at the More ❯

up to date, steering product development, and maintaining close working relationships with suppliers and their peers across organisational boundaries. The postholder will have responsibility for a team of 6 EPR Specialists who deliver change across our EMIS estate. As a team leader, the postholder must embody our values and take an active role in decision making both at local and … Optums EMIS product suite, and standardised coding systems such as SNOMED. Under the direction of the Head of Clinical Systems, input into development, and ensure the delivery, of an EPR optimisation programme of works to time and quality standards. Oversee change projects, including upgrades, relating to Optums EMIS product suite, providing advice and guidance to both direct reports and the … wider business on EPR matters. Represent Clinical Systems service line and input specialist knowledge into our change and project boards, supplier meetings, workshops, and management meetings as required or directed by the Head of Clinical Systems. Provide line management and professional support to a team of 6 specialists. Provide advice and guidance to the clinical systems technical team relating to More ❯

CD pipelines Familiar with observability tools, logging frameworks, and performance monitoring Desirable Skills: Background in serverless technologies (e.g. Lambda, Step Functions, API Gateway) Experience with data tools like EMR, Glue, or Apache Spark Understanding of event-driven architecture (EventBridge, SNS, SQS) Knowledge of AWS database offerings including DynamoDB and RDS Familiarity with multi-region deployments and failover strategies AWS More ❯

streams include but are not 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 collection technologies. Base Level: Bachelor … external data providers within a 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' experience managing data in support … with complex external data e.g., 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 global provider of clinical research More ❯

15+ years in data / analytics; 5 to 7+ years in leadership Hands-on expertise with modern data stack and ML platforms Experience in working with healthcare datasets (EHR, claims, wearables) Familiarity with international HIPAA, GDPR, and health data standards Strong stakeholder management in high-growth settings Degree in Data Science, Computer Science, or related discipline *This role More ❯

and evaluate their risks. You are a part of Philips CI&I Paris is in charge of a flagship product that manages information from medical devices and patient data to redistribute them to the different hospital systems (Electronic Medical Record, Monitoring ). You will work in the Edge Devices team who is More ❯

to act as Lead Digital (ePMA) Pharmacy Technician implementing, developing, and supporting all elements of the Trusts Electronic Patient Records (EPR) relating to prescribing and medicines usage and to work closely with the Pharmacy Department, IT department, EPR team as well as other Trusts using the same EPR system. Main duties … of the job Digital lead pharmacy technician implementing, developing, and supporting all elements of the Trusts Electronic Patient Record (EPR), under direction of the principal digital pharmacist, relating to prescribing and medicines usage and to work closely with the Pharmacy Department, IT department, EPR team as well as other Trusts using the same EPR … system. Assist with the implementation, maintenance and development of electronic prescribing and medicines administration (ePMA) across QVH. Support back-end technical processes such as configuration, development and testing of the Trust's current or future ePMA systems. Train and support all staff involved with the ePMA process. This includes pharmacy staff, prescribers, nurses and floorwalkers. Be a More ❯

to act as Lead Principal Digital (ePMA) Pharmacist implementing, developing, and supporting all elements of the Trusts Electronic Patient Records (EPR) relating to prescribing and medicines usage and to work closely with the Pharmacy Department, IT department, EPR team as well as other Trusts using the same EPR system. Main duties … the EPMA system, primary point of contact for risk management of the EPMA system, managing incidents, issues and clinical concerns. Act as an ambassador and clinical representative for the EPR and a champion for EPMA, engaging staff and promoting the benefits Person Specification Qualifications Essential registered pharmacist (GPhC) Independent prescribing post qualification diploma or able to demonstrate knowledge through experience … communication skills across all aspects Ability to motivate Ability to work across boundaries Ability to gather and analyse information and compile reports Apply risk management Take into account patient preference and protected characteristics Attributes Essential Innovative Identify and promote best practice Ability to communicate highly complex information to range of people Professional accountability Lead, develop and promote More ❯

can autonomously execute rigorous studies but also know when collaboration is key. 13. You know that ‘real-world data’ isn’t just one thing. You’ve worked across claims, EHR, registries, patient-reported outcomes, and more. You understand the strengths and limitations of each data source. 14. You know when a real-world study is the answer 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 in clinical data workflows. Maximize … Qualifications: Genuine passion for utilizing 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 pharmaceutical organizations. Proven experience in More ❯

Also Prior programming experience using 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 standards for a variety of real-world studies. Manage and contribute to quality … 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 More ❯