Project Data Manager (Medical Writing Team) Join to apply for the Project Data Manager (Medical Writing Team) role at Syneos Health Project Data Manager (Medical Writing Team) Join to apply for the Project Data Manager (Medical Writing Team) role at Syneos Health Project Data Manager … Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Description Project Data Manager Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate … customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work More ❯
We are seeking a Principal Data Scientist to be responsible and accountable for managing all DataManagement activities using advanced datamanagement tools and techniques with respect to cost, quality, and timelines for all assigned trials/projects within ClinicalData Acquisition and … Management. The position is a key collaborator and strategic partner with stakeholders ensuring that datamanagement activities for the clinical trials are executed efficiently with timely and high-quality deliverables (in alignment with the Novartis ClinicalData Quality Statement). This role reports to the … Director of Data Management. About the Role Key Responsibilities: Lead datamanagement activities as Trial ClinicalData Scientist for complex priority trial(s) or as a Project/Program ClinicalData Scientist for moderate complexity non-priority project(s)/program in study More ❯
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 an 9 to 12-month temporary contract. As a senior leader in the team, you'll play a critical part in designing streamlined, risk-based data strategies that drive … 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, stats, programming and monitoring, ensuring a cohesive, risk-based trial delivery approach Requirements Strong experience in clinicaldatamanagement with deep operational and technical More ❯
A global pharmaceutical company is currently looking for a Senior ClinicalData Manager to join their team on an 9 to 12-month temporary contract. As a senior leader in the team, you'll play a critical part in designing streamlined, risk-based data strategies that drive … 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, stats, programming and monitoring, ensuring a cohesive, risk-based trial delivery approach Requirements Strong experience in clinicaldatamanagement with deep operational and technical More ❯
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 ❯
Manchester, Lancashire, United Kingdom Hybrid / WFH Options
Arm Limited
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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 ❯
AI for the Pharma industry. The Instructional Designer needs to have a strong background in eLearning development and instructor-led training development. Expertise in clinicaldatamanagement or clinical trials would be a distinct advantage. The successful candidate will be responsible for designing, developing, and implementing … for both internal and external audiences. Key Responsibilities: Design, develop, and implement high-quality eLearning and ILT solutions for our software solutions serving the clinical trials industry, utilizing instructional design methodologies and eLearning authoring tools. Work closely with subject matter experts to ensure accurate and effective content development and … eLearning development. Strong knowledge of instructional design principles, adult learning theories, and eLearning authoring tools such as Articulate Storyline, Captivate, and Camtasia. Excellent project management, communication, and collaboration skills. Knowledge of clinicaldatamanagement or clinical trials would be a distinct advantage. Ability to work More ❯
risk, and optimize outcomes. More than one million registered users across 2,000+ customers and partners access the world's most trusted platform for clinical development, commercial, and real-world data. Known for its groundbreaking technological innovations, Medidata has supported more than 30,000 clinical trials and … help ensure that Medidata's software applications are implemented or enabled in accordance with Medidata standard business processes, meet client requirements and follow Good ClinicalDataManagement Practices. ICs also consult with our clients and provide guidance on how to best implement Medidata's software to provide … engagements, being accountable for quality of delivery. Support developers and other departments during configuration or implementation of specifications and issue resolution. Work to Project Management timelines and budgets, ensuring timely completion of deliverables within the agreed scope of work. Communicate status reports to stakeholders on both client and internal More ❯