Business Insights, Sr Associate (Remote)

Job Description
Purpose:
AbbVie aspires to build an industry leading data ecosystem, that can drive insight generation and operational efficiencies to deliver medicines to our patients safer and faster. In order to achieve this, we are designing a data strategy which includes a data governance structure and operating model that supports and drives a data driven organization.
The Sr. Associate, Business Insights (BI) role is a key technical support role to enable the application of advanced analytics across clinical development operations processes and identifying internal and external data trends to drive business value and actionable insights. This role will support the monitoring of these trends and identify underlying leading / lagging clinical trial performance indicators, in support of the BI team. This role will work across the Clinical Trial Management Ecosystem (CTME) and the executive dashboard (VISION) team to continuously enhance the existing ecosystem, driving cross-functional alignment with R&
D business functions andwith Business Technology Solutions (BTS).
Responsibilities:
Enables data-driven insights to support of BI and CDO activities
Partner with and support the BI team to proactively identify trending and review analytics to drive action steps
Communicate context, insights and objective analysis to BI team to support decision making
Present key findings and insights at BI team meetings with additional analysis as required, anticipating/identifying issues that could affect timelines or quality and develops options and solutions
Proactively work with relevant industry benchmarks / trends aligned to AbbVie’s pipeline
Maintain knowledge of current systems (i.E. Tesla, Veeva Vault, etc.) and alignment to existing business processes. ;
Support the business in ensuring proper ongoing use of the system, leveraging metrics and IR information to system use behavior is as intended;
Identify opportunities for process improvement and value creation by using objective data-based evidence
Bring critical insights for review in support of study team issues, anticipating/identifying issues that could affect timelines/quality and develops potential solutions
Conduct ad-hoc short-term consulting projects to answer critical questions from leadership
Ensures consistency on insight generation and analysis across assigned therapeutic area
Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development