Jobs at NAMSA

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.

The Associate Laboratory Services Specialist manages testing samples, maintains organization, performs administrative tasks, and communicates with various departments. Responsibilities include sample testing oversight, client interaction, and maintaining laboratory standards.

Prepare and process tissue samples and microscopic slides (paraffin, plastic, frozen), perform staining and QC, maintain GLP-compliant records and equipment, coordinate specimen shipping, assist with necropsies and specialized imaging, and train junior staff.

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

The Senior Clinical Research Associate manages clinical study responsibilities, ensures compliance with regulations, coordinates site monitoring, and supports trial activities and training.

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.

Execute human factors and usability activities for projects, develop protocols, perform data analysis, and draft regulatory usability reports.

The role involves performing routine testing, preparing test articles, recording data, operating lab equipment, and ensuring compliance with SOPs in a GLP/GMP environment.

Perform routine in vitro test article preparation and testing per SOPs; analyze and interpret data; maintain cell lines, reagents, equipment, and records; support environmental monitoring, cleanroom duties, autoclave operation, and quality systems (LIMS/Trackwise/MasterControl) in a GMP/GLP lab.

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.

The Study Director coordinates study tasks, oversees GLP/non-GLP preclinical studies, analyzes data, and ensures compliance with regulations. They act as primary client contact and manage project schedules and budgets while motivating team members.

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.

The Associate Study Director coordinates study tasks, serves as the client contact, ensures compliance with quality regulations, and evaluates study data and results.

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