The Toxicologist will prepare risk assessments, evaluation plans, and reports in compliance with ISO standards for regulatory submissions. They will also provide technical support to lab staff and advise clients on biocompatibility and material characterization issues.
The Director oversees clinical safety operations, including the management of adverse event reports and data monitoring committees. They also provide strategic medical consulting to clients and lead cross-functional teams to ensure project success and regulatory compliance.
The Toxicologist will prepare risk assessments, evaluation plans, and reports in compliance with ISO standards for regulatory submissions. They will also provide technical support to lab staff and advise clients on biocompatibility and material characterization issues.
The Associate Toxicologist will prepare risk assessments, evaluation plans, and reports in compliance with ISO standards for regulatory submissions. They will also provide technical support to lab staff and advise clients on biocompatibility and material characterization issues.
The Associate Medical Monitor performs medical review and interpretation of adverse events and device deficiencies to ensure clinical trial safety. They also provide medical expertise for clinical study protocols, regulatory submissions, and committee activities like CEC and DSMB.
The Clinical Study Manager is responsible for the end-to-end execution of clinical studies, including site selection, regulatory document management, and study tracking. They also collaborate with cross-functional teams to ensure project deliverables meet quality standards and regulatory requirements.
The Senior Clinical Research Associate manages clinical site monitoring activities, ensures adherence to Good Clinical Practice, and maintains study documentation. They also support study start-up, site selection, and regulatory submissions while serving as the primary point of contact for investigative sites.
The Safety Associate manages Individual Case Safety Reports (ICSRs), including intake, review, analysis, and data entry into safety databases. They also coordinate Clinical Events Committees (CECs) and Data Monitoring Committees (DMCs) while ensuring compliance with safety protocols and regulatory requirements.
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.
The Project Manager will partner with clients and cross-functional teams to manage project execution throughout the entire lifecycle, ensuring quality, schedule, and budget requirements are met. They will serve as the primary liaison for clients, facilitating project planning, financial management, and regulatory compliance.
The Field Senior Clinical Research Associate manages clinical site monitoring activities to ensure compliance with Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for investigative sites, supporting study start-up, enrollment, and data management tasks.
The specialist is responsible for assessing and auditing the compliance of biocompatibility and material characterization results against applicable standards. They will also develop and review complex biological safety documents and reports for medical devices.
