documentation in an audit-ready manner. Support Lead Clinical Programmers in developing and managing Data Transfer Agreements... to Clinical Study Teams to ensure data is reviewed and discrepancies are resolved. Collaborate with internal stakeholders to meet...
documentation in an audit-ready manner. Support Lead Clinical Programmers in developing and managing Data Transfer Agreements... to Clinical Study Teams to ensure data is reviewed and discrepancies are resolved. Collaborate with internal stakeholders to meet...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
from startup to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward...). Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
with at least 2 as a Lead. Strong knowledge of data management best practices & technologies as applied to clinical trials Solid... understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
from startup to archival with at least 5 years in lead role. for clinical development programs with medical devices leading toward...). Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design...
support to Clinical Study Teams to ensure data is reviewed and discrepancies are resolved. Oversee Data Management activities..., internal teams, and site staff. Support Lead Clinical Programmers in developing and managing Data Transfer Agreements. Lead...
import/export agreements and data specifications. Serve as lead CDM on assigned clinical trials by attending internal... guidance to clinical data management personnel on assigned projects, reviewing study documents as needed, e.g. Data Management...
documentation in an audit-ready manner. Support Lead Clinical Programmers in developing and managing Data Transfer Agreements... to Clinical Study Teams to ensure data is reviewed and discrepancies are resolved. Collaborate with internal stakeholders to meet...
Responsibilities: Leads, performs, and oversees data management activities for clinical studies and/or clinical... programs. Performs hands-on clinical data management tasks to support clinical studies, including, but not limited...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
from study start-up to database lock for assigned studies. Lead multiple large and complex studies, delegating tasks...Responsibilities: Maintain study-specific documentation, including Data Management Plans, eCRF specifications...
documentation in an audit-ready manner. Support Lead Clinical Programmers in developing and managing Data Transfer Agreements... to Clinical Study Teams to ensure data is reviewed and discrepancies are resolved. Collaborate with internal stakeholders to meet...
Responsibilities: Independently identify, prioritize, and lead all CDM activities for assigned study. Represent CDM... are actioned appropriately. End to end experience in all phases of a clinical study from a DM perspective: startup, maintenance...
thinking, alignment-building and discretion to tailor documents to study needs. Independently lead data cleaning activities...Responsibilities: Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
from startup to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward...). Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design...
from startup to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward...). Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design...