Associate Director, Clinical Data Reporting & Analytics

Working with Us
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Department Title and Description

Clinical Data Reporting and Analytics (CDR&A)

CDR&A is responsible for the ingestion, transformation, and delivery of clinical data to internal stakeholders, primarily to Biometrics and Data Sciences.  CDR&A also acts as the study interface for delivery of reports and analytics to enable effective data review, trial status and risk identification.  Engagement of clinical trial functions for reporting and analytic needs.  Technical SMEs to ensure expert consultation on data modeling, transformation, and best-fit reporting tools.

Purpose/Objective the job

This position is dedicated to the Reporting Innovation & Technology function within Clinical Data Reporting & Analytics.  The Associate Director, Clinical Data Reporting & Analytics to be responsible for identifying and driving opportunities for analytic support within the clinical data review community.  Interpret and translate business needs into tangible reporting solutions.  Drive the development and implementation of new reporting tools as applicable. This position reports to the Director, Reporting Innovation and Technology.

Key Responsibilities and Major Duties

• Interface/liaise with a variety of end users and can think holistically about data review approaches that will support Risk Based Monitoring, clinical review and other data related initiatives
• Can think strategically regarding broad scope analytic solutions, including appropriate infrastructure and technological requirements
• Leverage technical expertise to define feasible solutions and drive strategic use and implementation of new reports/visualizations, including any applicable training material
• Can proactively identify data review gaps in current processes and projects and lead/drive discussions to define new opportunities for data review tools
• Can interpret and translate a data review business need into a tangible report/visualization
• As required by business needs, able to lead large scale cross-functional projects which require strong stakeholder management and project management skills
• As required by business needs, able to operate effectively as a Line Manager in guiding a team of up to 10 Clinical Data Reporting & Analytics staff to deliver study level reporting solutions

Experience Requirements

• BS computer science, programming, data management, scientific or analytic discipline
• 7 years’ experience in the Pharmaceutical Industry focused in the clinical trial space
• At least 1 year in a leadership and/or supervisory role

Key Competency Requirements

• Experience with varied reporting and analytic tools, Spotfire, Tableau, elluminate, Qlik, JReview, SAS, and/or SQL
• Emphasis in Biostatistics a plus
• Strong understanding of relational databases
• Varied Therapeutic Area knowledge
• Strong analytic and problem-solving skills
• Proficient in stakeholder engagement and management
• Experience interacting with Informatics on large scale projects

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accounta