Top Pharmaceutical Operations & Support Jobs

The Executive Assistant will support four senior leaders by managing calendars, coordinating travel, office management, and fostering company culture. Must have 5+ years experience in a fast-paced environment, ideally biotech.

The Associate Director/Director of Quality Assurance for GCP will oversee quality activities related to clinical development programs, manage audits, ensure regulatory compliance, and lead quality initiatives across the company.

Coordinate all aspects of clinical trials ensuring adherence to ICH and GCP guidelines, assisting with data analysis, safety assessments, and managing patient involvement throughout the study process.

Oversee indirect sourcing and category management for Commercial and G&A, leading supplier selection, negotiations, and procurement operations.

Review batch records for accuracy and compliance, support manufacturing documentation processes, and assist with audits and trending analysis.

The Senior Resource Manager oversees resource management, staffing processes, and collaborates with leaders to optimize resource allocation and address staffing needs.

The role involves managing clinical samples for biomarker testing, coordinating with vendors, conducting data analysis, ensuring compliance, and contributing to clinical trial activities.

The LRMS Administrator manages the Laboratory Resource Management System, ensuring scheduling accuracy, resource allocation, and data integrity, while troubleshooting issues and liaising with laboratory operations.

The Senior Manager, IT Business Relationships serves as a liaison between Commercial teams and IT, ensuring technology solutions align with business needs and delivering value while managing initiatives and communication.

The Executive Assistant supports the CRDO by managing complex calendars, communications, and logistics, ensuring efficient leadership operations within R&D.