Data Management Services
Our team seeks to support our clients in achieving higher quality data and more dependable outcomes via the implementation of meticulous oversight and tried-and-true expertise.
At Metis, our Clinical Data Management mission is to elevate the sponsor, site, and patient experiences through deliberate planning and collaborative consultation. Our team seeks to support our sponsors in achieving higher quality data and more dependable outcomes via the implementation of meticulous oversight and tried-and-true expertise.
The strategic inclusion of Clinical Data Management in our service offerings reflects our commitment to providing Sponsors with top-tier support marked by flexibility and affordability. Metis consultants possess comprehensive expertise in clinical research, spanning Biotech, Pharmaceuticals, and Medical Devices. With consultants who have over two decades of industry experience, our primary objective is to swiftly and authentically align with our Sponsors’ unique objectives. We seamlessly integrate into study teams, delivering immediate value and expertise.
Core Data Management Services
Quality Data
Review & Cleaning
Operational oversight by functional experts; responsible for ensuring quality data is achieved via quality processes.
Oversight of traditional data management/data science activities
Represent Data Management on behalf of the Sponsor
Support fit-for-purpose vendor selection
Contribute to the negotiation and finalization of vendor contracts and budgets
Document review, input and alignment (DMPs, CCGs, DTAs, DRPs, etc.)
Vendor oversight, ensuring quality and adherence to contracted responsibilities
Audit conduct and support
Gap analysis of existing controlled documentation
Guide cross-functional review, input and interaction with clinical data
Implement custom reporting to support comprehensive data review and data cleanliness
Quality Data Capture
Technological oversight; responsible for the implementation of fit-for-purpose data acquisition tools and associated processes.
Certified builders
Oversight of GCDMP, CDASH and CDISC-compliant data capture tools
Support fit-for-purpose CDMS selection
Design protocol-specific Case Report Form drafts for delivery to CRO
Implement a CRF Global Library of Forms
Develop data collection standards (form, check, instruction)
Contribute to the negotiation and finalization of vendor contracts and budgets
Initial database builds and interim database modifications
URL Administration (Medidata Rave)
Oversee the implementation of new platforms within an organization
User Administration
Vendor oversight, ensuring quality and adherence to contracted responsibilities