Description
Responsible for data management activities on assigned protocols in
support of project goals.
Utilizes Oracle Clinical based data review tools, eDM (electronic
discrepancy management) and eDC (electronic data capture), to manage
clinical trial study activities.
Utilizes clinical data review applications (SAS) to create reports and
generate data listings.
Develops protocol standards and ensure standards are applied at the
protocol level throughout the course of a study.
Assists with training of data-related activities to investigators and/
or site personnel.
Requirements
Qualifications
Bachelors degree in Life Sciences, Allied Health, Pharmacy, Nursing or
related field of study. Advanced degree preferred.
Experience with Oracle Clinical Database or comparable Data Management
system.
Strong interpersonal and communication skills required.
Skilled in use of computer technology, including database management
systems, and ability to quickly learn new applications.
Overall understanding of ICH-GCP guidelines or regulations.
General understanding of project planning and management methods as
applied to clinical development programs.
Mail you cv to sigmas...@gmail.com