Remote Jobs at NAMSA
Find your next remote opportunity · 10 Open Positions
Helping medical device Sponsors improve healthcare since 1967, NAMSA is the world’s leading MedTech Contract Research Organization (CRO) offering global end-to-end development services.
Driven by its global regulatory expertise and in-depth therapeutic knowledge, NAMSA is dedicated to accelerating medical device product development, offering only the most proven solutions to move clients’ products through the development lifecycle efficiently and cost-effectively.
From medical device testing; regulatory, reimbursement and quality consulting; and clinical research services, NAMSA is the industry’s premier, trusted partner for successful development and commercialization outcomes.
Learn more: https://namsa.com/about/client-testimonials/
Toxicologist
Toxicologist preparing biocompatibility and toxicology assessments for NAMSA’s medical-device clients. Developing regulatory reports, advising clients, and supporting FDA submissions.
Associate Toxicologist
Associate Toxicologist supporting NAMSA’s medical-device safety and biocompatibility consulting. Preparing regulatory assessments, reports, and client guidance for global healthcare products.
Senior Clinical Research Associate
Senior Clinical Research Associate supporting NAMSA’s medical-device clinical trials. Managing site monitoring, regulatory documentation, audits, study metrics, and clinical research operations.
Clinical Study Manager
Clinical Study Manager leading medical-device clinical trials at NAMSA, a global MedTech development solutions provider. Managing sites, study deliverables, compliance, and cross-functional teams.
Clinical Research Associate – Internal Site Management
Clinical Research Associate ensuring Good Clinical Practice compliance through site monitoring for clinical trials. Collaborating with cross-functional teams and managing site communications effectively.
Supervisor, Global Client Success
Supervisor for Global Client Success team managing client interactions for medical device solutions. Ensuring effective client experience with laboratory submissions and NAMSA client portals.
Clinical Research Associate – Part time Contractor
Clinical Research Associate ensuring compliance with clinical regulations for medical device trials. Managing site monitoring and communication for clinical studies.
Biological Safety Specialist
Biological Safety Specialist ensuring compliance with medical device regulations. Developing safety documents and auditing biocompatibility results according to regulatory standards.
Clinical Field Specialist – Engineer
Clinical Field Specialist or Engineer at NAMSA specializing in medical device materials and product development lifecycle. Providing support for clients in global healthcare and regulatory environments.
Manager, Clinical Study Management
Manager, Clinical Study Management leading clinical studies for medical device testing compliance. Ensuring regulatory standards and collaborating with teams throughout the project lifecycle.
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