Teams at AstraZeneca

Field-based leader driving scientific engagement and KOL advocacy for the ATTR brand across the U.S. West. Partners with Medical, Brand, Sales, and Market Access to deliver compliant scientific exchange, surface field insights, lead regional/national initiatives, represent the brand at congresses, and use digital/CRM tools and analytics to improve engagement and inform strategy. Manages projects, vendor relationships, and cross-functional alignment.

Supports clinical study start-up activities from site selection through activation. Maintains tracking spreadsheets, logs, communication tools, and essential study documents; reviews Sub-Investigator and regulatory documentation; processes vendor access; monitors document workflows and activation risks; and provides status updates in study team meetings. The role follows ICH-GCP, company procedures, and applicable regulations while supporting timely, compliant, and cost-effective site activation.

Lead country-level clinical study start-up activities, including site activation, regulatory and ethics submissions, informed consent review, language negotiations, feasibility planning, documentation, and eTMF readiness. Serve as the primary site contact, maintain CTMS data integrity, monitor milestones and risks, and collaborate with clinical operations teams, CRAs, vendors, ethics committees, and health authorities to accelerate study activation and support compliant trial delivery.