Top Biotech Jobs in Raleigh-Durham, NC

The HR & People Programs Partner will support HR functions, execute talent management initiatives, and improve workplace culture at the Durham site.

As a Senior Research Scientist, you'll oversee statistical programming for cancer care research, provide expertise in data analysis, and collaborate with cross-functional teams.

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The Senior Manager, GMP Quality Assurance oversees compliance with regulatory standards in GMP activities, conducts audits, and integrates AI technologies for quality assurance improvements.

The Sales Director will lead the sales process to close partnerships with research sites, managing all sales activities including discovery and negotiation, while collaborating with Customer Success for onboarding.

The Senior Manager will oversee account alignment and data validation for vaccine contracts, ensuring accurate market share data, and will liaise with representative teams to resolve data issues.

The Senior Payroll Specialist oversees US payroll processing, supports EMEA payroll, ensures compliance, and drives cross-functional process improvement initiatives.

The role involves supporting commercial objectives by educating healthcare providers on Tempus oncology products through presentations and managing key relationships in oncology.

As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

The Clinical Trial Associate is responsible for managing vendor spreadsheets, participating in vendor management, and supporting study start-up processes in clinical trials.

Manage third-party IRT vendors and lead IRT system design, deployment, UAT, documentation, training, and ongoing performance/risk management. Coordinate with clinical teams, logistics, and biostatistics to implement protocol-driven IRT solutions and ensure regulatory compliance.

Create and maintain daily and long-range lab schedules, coordinate resources and testing priorities with cross-functional teams, ensure compliance with GMP/GLP/ICH, track status and resolve conflicts to optimize laboratory workflow.

Lead a team developing formulations and analytical methods for nasal and inhalation early‑phase products, ensure data integrity and cGMP compliance, mentor staff, manage lab resources and timelines, and support feasibility and Phase I/II programs.

Lead end-to-end development of orally inhaled and nasal drug products (sprays, DPIs, nebulizers), providing technical leadership across formulation, analytical and device integration, setting development strategy and control frameworks, managing cross-functional teams, client interactions, resource planning, portfolio delivery, and ensuring regulatory and quality compliance.