Description
Key Roles:-Ensure compliance with all safety requirements and design of all clinical data for the data processing system.
-Project Manager for Application & Report Development.
-Act as a Liaison between stakeholders.
-Elicit project scope, requirements gathering, and analysis for new applications/reports and enhancements to clinical data systems.
-Coordinate UAT and Training.
-Manage Applications/Reports roll-out and implementation.
-Provide systems support for Internal and External customers.
-Lead Process Improvement and Customer Experience Improvement initiatives.
-Assist in Study Setup in Oracle Clinical.
-Create Data Management Plan for the study and assist with data querying, data cleaning and database lock.
-Identify, create and track Ad-Hoc queries.
-Generate reports to assess data quality.
-Generate datasets for regulatory submissions.
Requirements:
-Bachelor's Degree in Computer Science, related field, or equivalent
-Experience within Clinical Data systems utilizing traditional paper CRFs and EDC functionality
-Experience with software development, testing and verification
-Demonstrated ability of relational database concepts
-Skilled in delegation, and good communication skills
This is an exceptional opportunity to make a difference within a team and a global organization by providing project management while creating reports to assess data quality. Please contact me immediately and send over your latest resume to be considered for an interview.
I look forward to hearing from you.
Best,
Joyce
Keywords:
Systems Analyst, GCP, FDA, Clinical Data Analyst, Los Angeles, California, Medical Device, UAT, CRF, Oracle Clinical, EDC, Regulatory
To find out more about Real please visit www.realstaffing.com