Support the preparation of technical and commercial proposals while collaborating with subject matter experts and operational teams to ensure alignment with client needs. Maintain opportunity tracking in Salesforce and assist in identifying potential laboratory and consulting opportunities to support regional sales objectives.
The pathologist serves as the study lead for nonclinical studies, ensuring compliance with FDA and international regulatory standards. Responsibilities include interpreting pathology data, collaborating with veterinarians, and preparing accurate protocol-driven reports.
The Research Associate is responsible for the quantification and measurement of core laboratory studies, including the review of echocardiograms and other imaging modalities. They will also participate in the development of quantification manuals and ensure adherence to industry standards and regulatory requirements.
Develop and implement targeted sales strategies to achieve goals within the Clinical and Consulting portfolio while managing key accounts. Orchestrate business review meetings and provide market analysis to drive sales growth and strategic development.
The Core Lab Project Lead assists with the development of regulatory documents, training materials, and study-specific procedures for multi-centered clinical trials. They also act as a liaison between various stakeholders and support core lab image processing, data entry, and billing activities.
The Senior Regulatory Consultant will lead the development and execution of global regulatory strategies for medical devices and related technologies. They will serve as a primary consultant to clients, managing regulatory submissions and providing strategic guidance to ensure market access and compliance.
The Associate Director provides scientific oversight for anatomic pathology evaluations and ensures all studies comply with GLP, FDA, and ISO regulatory requirements. They also lead regional pathology operations, manage staff, and collaborate with internal teams to optimize workflows and expand service offerings.
The Senior Clinical Research Associate manages clinical site monitoring activities, ensures adherence to Good Clinical Practice, and serves as the primary point of contact for site-related issues. They also support study start-up, regulatory submissions, and data management tasks to ensure high-quality clinical trial execution.
The Business Development Executive is responsible for developing and implementing territory sales strategies to position NAMSA as a premier Medical Research Organization. They will manage existing accounts, acquire new business, and collaborate with internal teams to deliver effective sales presentations and proposals.
