Coordination and management of clinical trial sites including but not limited to supporting the study start up process (assist in the collection of key regulatory documentation for submission to the IRB/EC, as well as assisting with budget and contract negotiations), routine site management, and site closure Conduct monitoring visits (Site Initiation Visit, Interim Monito

Provide multi faceted support to day to day marketing operations, such as media campaigns, promotions, and event planning and coordination. Support social media and PR activities to include digital support (support website logistics). Submission of purchase orders and invoices for approval and payment, as requested. Support of patient advocacy activities including Breast

Identify, target, educate and manage accounts in the assigned territory including hospitals, pathology groups, oncologists, and surgeons on Agendia's products. Analyze the designated territory to understand prescribing and purchasing decision processes and any marked differences from national trends Drive new oncology business, maintaining customer relationships and excee

o Maintains and improves the Agendia QMS [compliance with FDA, IVDR, CLIA, ISO, etc.]. o Ensures applicable standards and regulations pertinent to Agendia are effectively implemented and acts as an advisor to all managers. o Leads development of regulatory submissions. o Provides support to currently marketed products as necessary labeling, product changes/documentation.