Top Biotech Data & Analytics Jobs in Boston, MA

The Director oversees Market Access strategies, focusing on pricing, contracting, and reimbursement through advanced analytics. Responsibilities include stakeholder alignment, financial modeling, and cross-functional team collaboration to enhance patient access and support business growth.

The Bioinformatics Scientist analyzes lab-generated data, creates computational models, and develops tools for NGS data analysis, while collaborating with teams.

The Advanced Data Analytics Lead will drive data-driven decision-making in the pharmaceutical sector, lead project teams, develop client relationships, and leverage data analytics and AI solutions to tackle complex business problems.

The Senior Analyst, People Analytics will enhance data accuracy and usability across HR processes, manage audits, and deliver operational reporting.

The Senior Director, Business Analytics leads enterprise analytics for Scholar Rock's commercial launch, defining strategies that support decision-making and growth initiatives.

The Manager, Data Science - Oncology will lead data engineering initiatives, optimize workflows, and support data projects, specifically in Oncology R&D. Responsibilities include developing data pipelines, managing a technical team, and collaborating with stakeholders to deliver data solutions.

The Senior Manager, Customer Analytics drives analytics to inform commercial strategy, supports data management, and enhances reporting for the business.

The Senior Data Manager oversees all data management activities for clinical trials, ensuring data quality, consistency, and compliance while mentoring team members and collaborating across departments.

The Data Solutions Engineer will design and deliver data and analytics solutions, manage data pipelines, and support cloud platforms while collaborating with various teams to improve data accessibility and operational efficiency.

The Principal Statistical Programmer will generate and validate datasets, oversee deliverables from CROs, and ensure compliance with standards for clinical trials in a pharmaceutical setting.