3 of 3 Permanent Clinical Data Management Jobs in the North West

Senior Clinical Research Data Manager

Hiring Organisation
UKHCDO
Location
Salford Quays, M50 3YJ, United Kingdom
Salary
£49387.00 to £56515.00
summary The postholder will translate study protocols and research questions into practical, proportionate data-collection requirements, including the design and refinement of study-specific Case Report Forms (CRFs), database modules, worksheets, data management plans and completion guidance. They will work closely with participating haemophilia centres to facilitate … data collection, resolve operational difficulties and ensure that study data are complete, timely, consistent and suitable for analysis and reporting. The role has three core components: Study-specific data management: Developing and maintaining the additional data-collection tools and processes required for post-marketing ...

Senior Clinical Research Data Manager

Hiring Organisation
UKHCDO Limited
Location
Salford, Greater Manchester, North West, United Kingdom
Employment Type
Permanent
Salary
£55,000
Title: Senior Clinical Research Data Manager Location: Salford Quays Salary: £49,387- £56,515 per annum - Band 7 Contract: Full time, Permanent About the Role: The National Haemophilia Database (NHD) is the UK's national registry for people with inherited and acquired bleeding disorders, collecting clinical and treatment data from NHS haemophilia centres across the UK. We are seeking an experienced Senior Clinical Research Data Manager to provide specialist data management and coordination for post-marketing studies, investigator-initiated studies and other approved research delivered through the NHD. Working with ...

EDC Clinical Trial Designer - FSP (Homebased - UK)

Hiring Organisation
IQVIA
Location
Manchester, Greater Manchester, United Kingdom
Salary
£ 50 K
Clinical Trial Designer will create high quality data collection tools for new clinical trials and facilitate activities related to the design, development, documentation, testing and implementation of clinical eCRF databases. Design of eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio … expected. In addition, the EDC Clinical Trial Designer will ensure that all relevant standard operating procedures, CRF Standards, process and trial-specific guidelines are implemented and utilized to help ensure that a quality work product is produced and timelines and deliverables are consistently met.Summary of the Essential Functions ...