Jobs at NAMSA

The Senior Clinical Research Associate coordinates clinical site monitoring, ensures compliance with regulations, and manages clinical trial documentation, training, and site relations.

Perform routine accounts payable tasks including invoice verification, purchase order and terms reconciliation, supplier communication, GL coding, outgoing payments, supplier statement reconciliation, and use tax recording to ensure timely, accurate payments.

Perform routine microbiology test article preparation, execute tests per NAMSA SOPs, record and review data, operate laboratory equipment, perform environmental monitoring and cleanroom maintenance, respond to monitoring alarms, support test specification preparation and client interactions, and follow GLP/GMP and applicable standards.

Support and coordinate preclinical medical device studies from initiation through completion, serve as Study Director for GLP and non‑GLP studies, prepare IACUC protocols, ensure regulatory and quality compliance, analyze and report data, interact with clients and regulatory bodies, and perform study procedures as needed.

Support Study Directors/Principal Investigators in GLP and non-GLP preclinical studies by coordinating study tasks, collecting and entering data, maintaining records and test article accountability, communicating with sponsors and investigators, assisting with protocol generation and technical reports, and managing study documents and logistics.

Provide clerical and technical support for laboratory studies: review raw data and photos, update SOPs/protocols/worksheets, generate IACUC submissions, maintain study spreadsheets, initiate nonconformances, interact with clients/auditors, assist scheduling, and meet on-time metrics.

The Client Success Program Manager serves as the main contact for clients, managing complex programs, resolving issues, and ensuring effective communication across teams to enhance client experiences.

Performs necropsies, routine gross examinations, tissue trimming, specimen shipping, photography and x-ray imaging, and maintains GLP-compliant records, SOPs, and laboratory equipment. Assists with protocol review, calibration/validation of specialized equipment, and other pathology-support duties.

As a Senior HR Business Partner, you will lead HR initiatives, support recruitment, mentor staff, analyze workforce data, and ensure compliance in HR practices while collaborating with senior management.

Perform routine in vitro test article preparation and testing per SOPs, maintain cell lines/reagents and lab records, conduct environmental monitoring and operate equipment, draft technical documents, ensure GMP/GLP compliance, respond to alarms, and support quality and workflow improvements.

Perform internal and supplier audits and inspections to assess compliance with GLP/GMP/ISO and SOPs; review lab records and data for accuracy; investigate quality issues, recommend improvements, and follow up on corrective actions.

The Microbiology Technologist performs routine testing and product preparation, accurately records data, monitors lab equipment, and maintains cleanroom environments as per SOPs.

The Principal Lab Technician is responsible for test article preparation, executing routine tests, conducting data analysis, maintaining lab supplies, and adhering to regulatory guidelines in a GMP/GLP environment.