Lead the day-to-day functions of a core Data & Analytics team providing centralized data coordination and data analysis services for a large research portfolio
Directly oversee a small, dedicated team (including a Clinical Data Manager and a Data Management Analyst) supporting a robust portfolio of 65+ active multi-site research studies
Manage the day-to-day data management and analysis pipeline
Act as the Subject Matter Expert (SME) for internal and external stakeholders
Execute on your own data management, quality control (QC), and data analysis activities
Ensure the on-time execution of high-quality and compliant research, proper documentation of procedures, accurate data reporting, and assure real-time data access for the investigator(s) and staff
Provide regular summaries and updates to Program Supervisor
Plan and facilitate individual and team meetings
Lead performance review processes for assigned data team staff
Supervise the day-to-day activities of assigned data management & analytics team program staff
Maintain oversight of data management and analysis needs across a large portfolio of clinical research studies, effectively delegating tasks and tracking project timelines
Lead and mentor a team of data professionals
Act as a hands-on backstop to execute technical tasks (e.g., database builds, QC cycles, dashboard creation) during team absences or high-volume periods
Oversee the drafting, application, and compliance management of Data Sharing Agreements (DSAs) and Data Use Agreements (DUAs)
Requirements
Bachelor's degree in a scientific, informatics, or relevant field required
Master's degree, equivalent work experience, or relevant professional certification strongly preferred
3-5 years' professional experience in clinical research data management, clinical trials, or a data coordinating center environment required
Previous research conduct experience highly desired
1-2 years in team management, leadership, or direct supervisory experience required
Must possess a strong working knowledge of clinical research data compliance, including requirements for FDA-regulated clinical trials, IRB requirements for human subjects protections, and general best research practices
Must have demonstrated experience building complex, longitudinal, multi-arm electronic clinical research databases required
Experience using REDCap is strongly preferred
Must have demonstrated experience with cleaning, analyzing, and presenting real-time data and metrics
Must have a strong understanding of data visualization principles and the ability to build or troubleshoot business intelligence dashboards
Experience with PowerBI strongly preferred
Experience executing or navigating data agreements (e.g. data use agreements, data sharing agreements, etc.) as they pertain to data privacy and security is highly desired
Must be organized, attentive to details, and possess exceptional diplomatic and professional communication skills
Must have the ability to successfully build relationships with key stakeholders and to effectively communicate requirements for data and analytics systems as well as translate technical data requirements to non-technical stakeholders
Must thrive in a fast-paced environment with shifting priorities, multiple moving targets, and strict timelines.
Benefits
medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution