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SENIOR MANAGER, CLINICAL DATA REPORTING AND ANALYTICS LAWRENCEVILLE, NJ 50% onsite (Hybrid). Project Description:
- Global Data Management and Centralized Monitoring/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.
- This position is dedicated to the Reporting & Analytics Delivery function within Clinical Data Reporting & Analytics.
- The Senior Manager, Clinical Data Reporting & Analytics to be responsible for identifying and driving opportunities for analytic support within the clinical data review community.
- Serve as a primary report delivery contact for stakeholders including data management, clinical data reviewers and physicians.
- Interpret and translate business needs into tangible reporting solutions.
- Drive the development and implementation of new reporting tools as applicable.
- 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.
- Can create/develop prototypes for new solutions as applicable.
- As required by business needs, able to lead large scale cross-functional projects which require strong stakeholder management and project management skills.
- BS computer science, programming, data management, scientific or analytic discipline with 5-7 years' experience in the Pharmaceutical Industry focused in the clinical trial space.
- Experience with varied reporting and analytic tools, Spotfire, Tableau, Qlik, JReview, SAS, and/or SQL.
- Strong understanding of relational databases.
- Varied Therapeutic Area knowledge.
- Strong analytic and problem-solving skills.
- Proficient in stakeholder engagement and management.
- Emphasis in Biostatistics a plus.
- ID: #49470835
- State: New Jersey Lawrenceville 08648 Lawrenceville USA
- City: Lawrenceville
- Salary: BASED ON EXPERIENCE
- Job type: Contract
- Showed: 2023-03-14
- Deadline: 2023-05-12
- Category: Science/biotech