Top Tech Jobs & Startup Jobs

The Senior Manager, Regulatory Affairs will oversee regulatory strategies, manage submissions to the FDA and international agencies, and coordinate with cross-functional teams to ensure compliance and timely submissions.

The Director of IT Quality & Compliance manages IT compliance and validation, overseeing Veeva Vault Quality and ensuring IT systems meet regulatory standards while collaborating with QA teams.

As Director of AI Enablement, you will lead Apogee's AI strategy, managing program operations, cross-functional collaboration, governance, and performance measurement to drive organization-wide AI literacy and adoption.

Manage logistics of biomarker sample collection, ensure adherence to clinical protocols, oversee data transfer, vendor management, and budget tracking for clinical trials.

The Senior Manager of Clinical Systems oversees clinical technology initiatives, manages clinical systems projects, ensures compliance, and promotes process adoption across multiple functions while collaborating with various stakeholders.

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.