36 Edc Systems Jobs - Page 2

At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. We are seeking a dynamic Manager to join our Life Sciences Consulting team, specializing in Clinical Operations transformation. This role involves working with global pharmaceutical, biotech, and medtech clients to optimize R&D and clinical delivery models, streamline operations, and implement emerging technologies across clinical developmen...

You should have at least 2 years of experience in Clinical Trial EDC, preferably with systems like Veeva, RAVE, or Oracle, and/or Reporting experience, preferably with tools like JReview, Spotfire, Jupyter Labs, or SQL. You should be familiar with common troubleshooting tools and technologies such as JIRA, Dynamics, and have a good understanding of Microsoft Office products like Office, Excel, PowerPoint, and Dynamics. It would be ideal if you have an understanding of web technologies and web services like RESTful APIs, SOAP, and experience with database technologies such as Java, Python, and SQL, for troubleshooting issues related to cloud-based software systems. In addition to technical sk...

Are you ready to make a significant impact in the world of Biopharma Clinical Operations As an Associate Director in GCS Business Technology Solutions, you'll be at the forefront of driving industry-leading processes, technology, and services. Your role will be pivotal in owning the lifecycle management and continuous improvement of specific clinical operations processes, systems, or services. Collaborate with internal and external stakeholders to ensure customer needs are met and optimize the delivery of clinical studies. You'll identify and deliver improvements using tools like Lean Six Sigma to improve clinical study delivery. Are you up for the challenge Design, develop, implement, maint...

As the EDC Systems Specialist, your primary responsibility will be to design eCRF layouts and databases in alignment with EDC systems. You will be tasked with setting up core configurations in Medidata Rave or other EDC platforms. It is mandatory for you to implement dynamic rules and custom functions using C# as per sponsor requirements. Additionally, you will create, test, and maintain edit checks based on Data Validation Specifications. Your role will involve incorporating internal feedback and SAT feedback from sponsors to enhance the eCRFs and components for protocol amendments and metadata updates. You will perform a second/final peer review of deliverables to ensure accuracy and compl...

At EY, you will have the opportunity to shape your future with confidence, succeed in a globally connected powerhouse of diverse teams, and take your career wherever you desire. Join EY to help build a better working world. As a Data Integration Architect with 8+ years of experience in clinical or life sciences domains, you will lead the integration of Medidata platforms into enterprise clinical trial systems. Your role will involve designing scalable, compliant data integration solutions, collaborating across global R&D systems, and contributing to data-driven innovation in the healthcare and life sciences space. You will play a crucial part in aligning integration efforts with organization...

As a Manager in GCS Business Technology Solutions at AstraZeneca, you will play a crucial role in leading and innovating in the realm of Biopharma Clinical Operations. Your primary responsibility will be to design, develop, and continuously improve processes, systems, and services that drive clinical study delivery. You will collaborate with internal and external stakeholders to meet customer needs and enhance the efficiency of clinical studies. Utilizing tools like Lean Six Sigma, you will identify and implement improvements to ensure optimal end-to-end delivery. Are you ready to make a difference in this dynamic and challenging role Your key accountabilities will include designing, develop...

The Clinical Data Manager is responsible for overseeing all data management activities pertaining to the conduct of Phase I-IV clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met. Participate as the primary data management representative on the QED multidisciplinary project teams and as the primary point of contact for all data management interactions with the Sponsor. Participate in protocol developments and review, in review of clinical study reports and statistical analysis plan, in the development of data dictionaries complete with variabl...

You will be responsible for creating a catalogue of reports to support data cleaning activities with low to medium complexity. Your tasks will include automating manual checks, reconciliation, and program edit checks for TPV data to ensure quality. Additionally, you will develop tools and repositories to minimize data errors at the source for the collection of lab reference ranges. You will program reports to identify missing pages, detect errors at the Subject level, and create reports to measure metrics for assessing data cleaning status. Furthermore, you will be tasked with creating visualizations and dashboards to identify discrepancies and trends in EDC and TPV data. In addition to the ...

As a Clinical Database Programmer at ProcDNA, you will play a crucial role in designing the eCRF layout and corresponding database, implementing dynamic rules based on Sponsor requirements, and creating trial-specific Edit Checks. Your responsibilities will also include developing Custom Functions using C# for Rave studies or other EDC systems, incorporating internal and Sponsor feedback, and maintaining eCRFs and components as per protocol amendments or metadata updates. Additionally, you will support CRO trial activities, create reports using JReview, SAS, BOXI, and handle migration processes for Post Go-Live studies. To excel in this role, you must have a deep understanding of Clinical Pr...

Responsibilities include, but are not limited to, the following: Support of clinical trial platform technologies Support decision-making by acting as a data scientist bringing awareness to patterns and analytical insight. Coordinating and providing programming support to Clinical Study Teams Ensure efficient and consistent use of EDC system and ensure the use is complied with the established procedures or standards. Acting as a technical point of contact for systems deliverables on defined programs Identify, recommend or implement system enhancements, new tools or emerging technologies to decrease database development cycle times and foster a collaborative working environment. Providing tech...

Manager, CSAR - Electronic Data Interchange and Acquisition Role Description The Manager, CSAR - Electronic Data Interchange and Acquisition will report to the Sr. Manager, Clinical System and Analytical Reporting, focusing on Electronic Data Interchange/Acquisition programming activities. This role involves developing the Data Acquisition Requirements Specification (DARS) document to outline metadata transfer requirements, establish and validate vendor integration criteria, and manage the processing of electronic data from vendors. The position requires cross-functional collaboration to ensure high-quality deliverables, support clinical systems, and oversee electronic data capture technolog...