Lead global initiatives for document control, archives, and training, ensuring compliance with regulatory requirements and overseeing systems and staff in these areas.

Seeking a motivated Scientist to develop regulatory-ready bioanalytical methods using LC-MS. Responsibilities include sample preparation, analysis, and method optimization while ensuring compliance with standards.

The Quality Control Associate reviews and validates clinical trial data to ensure compliance with protocols and regulatory guidelines, identifies errors, and assists in scheduling appointments.

The Administrative Assistant supports the training department by coordinating onboarding, managing LMS tasks, preparing training materials, and maintaining documentation.

The Scientist will manage and conduct method development, validation, and sample analysis; serve as a key contact for client projects and ensure compliance with protocols and guidelines.

The Senior Scientist will oversee immunoassay study conduct, manage project timelines, mentor junior staff, and ensure compliance with regulations.

The QC Reviewer is responsible for quality control of data in the laboratory, ensuring proper documentation, compliance with SOPs, and mentoring analysts while addressing quality issues and trends.

The Study Design Specialist reviews study protocols and creates study designs in Watson LIMS, manages sample discrepancies, and supports sample management while ensuring compliance with SOPs and GCPs.

The Business Associate supports Business Development by generating leads, conducting outreach, documenting communications, and assisting with client engagement.

The Senior Payroll Administrator processes full-cycle payroll for Canada, conducts audits, oversees payroll coordinators, and ensures compliance with payroll regulations.