Back to jobsProvides data coordination and data management for randomized clinical studies.
Manages investigative site activity for multiple protocols.
Coordinates budgets and invoicing
Creates and implements subject enrollment strategies for assigned investigative sites.
Ensures clinical trials are managed and executed following ICH GCP, regulations, the protocol, and company-specific SOPs.
Designs CRFs and eCRFs for data acquisition and data entry.
Works closely with sites to train and support data capture and cleaning, coordinating efficient corrections to the database, assisting with troubleshooting and site challenges.
Defining necessary validations or reports to ensure quality and timeliness of data collection.
Monitoring study metrics and site performance using standard study management tools.
Collaborates with the study team to prepare abstracts, manuscripts, and other materials for internal and external audiences.
Participates in meetings with multidisciplinary teams both internally and externally to ensure successful and timely completion of deliverables.
Supports reporting to clinicaltrials.gov including data review, quality control checks, and interim and final analysis.
Ability to understand the objectives of a study and ensure that the databases, study case report forms, and data analysis match the overall study goals.
