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The Clinical Study Associate Manager oversees clinical trial delivery, ensuring compliance with regulations and effective collaboration with vendors. Responsibilities include planning, risk assessment, monitoring data quality, and managing study-related tasks and reports.

Lead and manage IT/OT operations in a GxP-regulated environment, ensuring reliable infrastructure (servers, networking, WiFi), compliance with FDA standards, integration of IT and OT systems, vendor management, disaster recovery, and performance reporting while mentoring a technical team.

Lead design and deployment of a regulated QC lab orchestration layer connecting instruments, middleware, and enterprise systems. Define integration patterns, ensure scalability, resilience, and data integrity (GxP/21 CFR Part 11/Annex 11). Translate QC processes into automated workflows, enable sample lifecycle automation, evaluate vendors, support validation and incident resolution, manage budgets and vendor relationships, and drive the connected lab roadmap.

The Associate Director, Thought Leader Liaison will engage with oncology thought leaders, enhancing business discussions and implementing strategic initiatives within the Oncology Solid Tumor portfolio.

The Oncology Account Specialist engages HCPs to drive product revenue through account management and compliance, focusing on NSCLC/NMSC patients in key institutions.

The Clinical Study Associate Manager oversees clinical trial execution, manages vendor relationships, monitors study progress, and ensures compliance with regulations while mentoring staff.

Lead the design and governance of OT data systems for real-time decision-making. Ensure data quality and security while mentoring junior engineers.

The Associate Director, Government Pricing oversees compliance with pricing regulations, including submitting reports, analyzing pricing trends, and communicating with internal teams. Responsibilities also include monitoring pricing legislation and performing detailed calculations to ensure accurate submissions to government agencies.

The Director of Resource Management oversees strategic resource planning and management in research and development, ensuring efficient utilization of resources and leading a team of resource managers.

The Associate Manager in Research Program Management coordinates projects through the drug discovery pipeline, managing interdependencies and driving communication among cross-functional teams.