Top Tech Jobs & Startup Jobs in Boston, MA

The Associate Director, Analytical Development will lead activities related to analytical methods for biologics, manage experiments, and collaborate with cross-functional teams, while ensuring compliance with quality and regulatory standards.

The Director of Clinical Development will oversee clinical trials in inflammation and immunology, collaborating with cross-functional teams, ensuring protocol adherence, and providing scientific insights for decision-making.

The Director of US Insights and Market Development will lead market research initiatives, develop strategies for pre-launch and brand activities, and integrate insights from various analytics to support decision-making within the Commercial team.

Lead the biostatistics efforts for clinical studies, providing technical guidance, statistical analysis, and overseeing CRO teams while ensuring regulatory compliance.

The Executive Director of GMP Quality Assurance oversees the GMP QA strategy, ensuring compliance with global regulations, leading a high-performing team, and preparing for regulatory inspections and audits.

Lead design, planning, execution, and quality oversight of clinical trial data management (Phase I-IV). Manage CROs and vendors, ensure EDC/eCRF/ CDM standards, support database locks/snapshots, collaborate with Biostatistics/Programming and other functions, and maintain regulatory-ready documentation for submissions.

The Associate Director oversees CRAs managing CRO monitoring for clinical trials, ensuring compliance, performance, and process development while leading teams and managing training.

The Senior Associate in Regulatory Affairs supports FDA and global regulatory submissions, maintains regulatory data, coordinates with teams, and ensures compliance with submission standards.

The Senior Director of Commercial Strategy will lead the development and execution of the U.S. commercialization roadmap, collaborating with cross-functional teams and managing competitive intelligence processes.

The Associate Director will optimize clinical operations standards, enhance operational efficiency, and manage resources for global clinical trials, ensuring best practices and vendor performance.