The Senior Clinical Research Associate manages clinical site monitoring activities, ensures adherence to Good Clinical Practice and regulatory guidelines, and serves as the primary point of contact for study sites. They also support study start-up, data management tasks, and assist in the development of clinical protocols and study operations.
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 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 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.
