Liverpool, Merseyside, North West, United Kingdom Hybrid / WFH Options
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ClinicalData Manager – £35,000-£47,000 per annum– Liverpool/Hybrid The Role Do you have a keen eye for detail and a knack for ensuring data accuracy? Are you excited about using cutting-edge AI to transform healthcare? MyCardium AI, a rapidly growing company using … AI to revolutionise cardiac MRI analysis, is seeking a highly motivated ClinicalData Manager to join our team in Liverpool. In this pivotal role, you will oversee the collection, management, and analysis of imaging data from clinical trials. You'll ensure data quality and … integrity, working closely with a dynamic team to achieve our mission of improving patient outcomes. Key Responsibilities: Develop and manage data systems for imaging studies. Ensure adherence to regulatory standards and study protocols. Collaborate with investigators and statisticians to define data collection needs. Oversee data entry and more »
Proclinical is seeking a dedicated individual for the role of Associate Director, ClinicalData Management. The successful candidate will be responsible for leading the team and overseeing the execution of clinical trials. Responsibilities: - Organise and conduct team meetings. - Foster team development and identify high-performance team members. … Collaborate with the (Senior) Director ClinicalDataManagement on team development. - Provide guidance to project teams on the oversight and supervision of CRO/third party vendors and organize trainings as needed. - Act as a mentor for new team members. - Contribute to the development and review of … portfolio documents (includes contracts, guidelines, budgets, metrics, KPIs). - Ensure compliance with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. Key Skills and Requirements: - Extensive knowledge of ClinicalDataManagement with a focus on DM activities as a Lead more »
Proclinical is seeking a dedicated individual for the role of Associate Director, ClinicalData Management. The successful candidate will be responsible for leading the team and overseeing the execution of clinical trials. Responsibilities: - Organise and conduct team meetings. - Foster team development and identify high-performance team members. … Collaborate with the (Senior) Director ClinicalDataManagement on team development. - Provide guidance to project teams on the oversight and supervision of CRO/third party vendors and organize trainings as needed. - Act as a mentor for new team members. - Contribute to the development and review of … portfolio documents (includes contracts, guidelines, budgets, metrics, KPIs). - Ensure compliance with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. Key Skills and Requirements: - Extensive knowledge of ClinicalDataManagement with a focus on DM activities as a Lead more »
Job title : Senior Data Manager Job Type: Permanent Location : Cambridge/Remote (May have to travel to the Cambridge office on occasion) Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative … treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe and debilitating disease areas. Our guiding principles, centred around Integrity and Patient-Centricity, are at the heart of everything we do. Job Purpose Lead all ClinicalDataManagement … proposes mitigation strategies. Communicates study timelines and deliverables to the study teams and follows up to ensure timely delivery. Accountable for delivery of quality data for project milestones, decision analysis and database locks. Participates in Service Provider selection, evaluation and management, including reviewing and providing input to scope more »
India, Denmark, UK, Singapore etc. (www.tech-observer.com) We are hiring for following roles on FSP: a. Statistical programmers : 5-8 years of exp in clinical SAS Programming Senior Statistical Programmers : 8-12 years of exp in clinical SAS Programming b. Principal Statistical programmers : 12+ years of exp in … clinical SAS Programming Location -United Kingdom (candidates eligible to work in UK shall be considered) Work Timings : US Timings (EST -3 days and PST -2 days) Job Responsibilities- 1.Compliance with working SOPs within the framework of the Quality Management System and to Good Clinical Practice (GCP). … 3. Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines). 4. Review and interpret Report and Analysis Plans and provide comments for assigned projects. 5. Develop and review SAS programs and more »
Proposition development identify gaps in the market and key customer problems to develop propositions leveraging Cognizants process and technology expertise Solution Development and deal management Among the critical tasks will be to lead/support solution development for qualified opportunities in Life Science sector . This will mean working … process challenges in this space and translating the needs in developing compelling technology-based business process solutions. Specific areas of capability need to be: Clinical Services ClinicalDataManagement BioStats & Statis Programming Safety Services Pharmacovigilance Complaints Management Regulatory Services Regulatory Operations Medical Writing Commercial Services … Marketing & Sales Contract Management Solution Development Experience in developing solutions ground up, in partnership with different stakeholders within an organisation. Hands on participation in solution and content development Ability to lead and work in diverse, multi-functional teams Global Experience Significant international experience required working with pharma companies across more »
