With little supervision, work with the research team to complete the database build specs and create eCRFs in the EDC system (such as TrialMaster, REDCap, etc.) according to project deadlines
Gather User Acceptance Testing (UAT) results, then make any necessary database modifications until all problems are fixed
Address system/software issues by helping the team with debugging and troubleshooting tasks
Identify and implement any project-specific roles and permissions as appropriate by working with the project and system administration teams
For the objectives of project management and checking data integrity, create standard and ad hoc query reports
Provide reports for assigned research and projects, containing listings, summary tables, and visuals
Participate in the creation of strategic plans for new initiatives and facilities, and provide advice on database best practices
Participate in developing protocols and best practices for putting data standards into effect
Ensure adherence to the rules and guidelines for data management and data systems that apply both internally and externally, such as good clinical practice (GCP), Food and Drug Administration (FDA), and organizational standard operating procedures (SOPs)
Consult with users and instruct them on how to use the systems and tools for clinical trials
Job Requirements:
Bachelor s/Master s degree in Engineering, Computer Science (or equivalent experience)
At least 3+ years of relevant experience as a database builder
Extensive experience working with Data Extraction and Database Administration
Prior experience working in the pharma and biotech industry is nice to have