Reading, Oxfordshire, United Kingdom Hybrid / WFH Options
IQVIA Argentina
Provides datamanagement support, oversight, and/or accountability for one or more clinical trials. Lead collaboration with trial customers and internal/external partners to establish, align, and confirm datamanagement expectations. Create, plan, and track content, format, quality, and timing of datamanagement deliverables such as CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan, and archival. Gather content and integration requirements for eCRF and other data collection tools in collaboration with trial customers and functional partners. Establish conventions and quality expectations … for clinical data. Define expectations for dataset content and structure. Set timelines and follow-up to ensure timely delivery of all DataManagement milestones. Perform trial-level oversight controls as described in the oversight plan, QC process, and work instructions with minimal DML direction. Create clinicalMore ❯
A global pharmaceutical company is currently looking for a Senior ClinicalData Manager to join their team on a 9 to 12-month temporary contract. Role Overview As a senior leader in the team, you'll play a critical part in designing streamlined, risk-based data strategies … archive. You'll collaborate across functions and help shape the future of trial delivery. Key Responsibilities Lead the creation of an agile, tech-driven datamanagement operating model aligned with best practices. Evaluate and implement emerging technologies (EDC, integration platforms, analytics tools) to modernise data workflows. Embed … regulatory standards and quality-by-design principles across all datamanagement activities. Act as a strategic partner across clinical operations, statistics, programming, and monitoring, ensuring a cohesive, risk-based trial delivery approach. Requirements Strong experience in clinicaldatamanagement with deep operational and technical More ❯
the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Job Function: Data Analytics & Computational Sciences Job Sub Function: Biostatistics Job Category: Scientific/Technology All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom Job Description: The … Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and reporting solutions. The role requires proven technical capabilities in leading clinical trial activities and teams in accordance with departmental processes and procedures. The position is responsible … for overseeing or developing clinicaldatamanagement trial activities of moderate to high complexity. Responsibilities include data model specifications, data stream integrations, transformation of source to internal data models, and/or creating CDISC submission-ready SDTM tabulation packages (such as aCRF, define.xml, cSDRG More ❯
Job Description ClinicalData Scientist – Pharmaceutical/Clinical Trials/RWE Are you a dedicated ClinicalData Scientist with a passion for advancing pharmaceutical research? This role offers a unique chance to be at the forefront of groundbreaking clinical studies, where your expertise will … with benefits The Environment… - Innovative Solutions: Be at the forefront of advancing drug development through cutting-edge Electronic Health Records (EHR) technology, which accelerates clinical trials and improves patient outcomes globally. - Professional Growth: Join a highly experienced and collaborative Executive Team, offering ample opportunities for career development and leadership. More ❯