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.

Conducts remote and onsite monitoring for clinical trial sites, including site qualification, study start-up, risk-based monitoring, source data review, safety reporting, investigational product accountability, recruitment tracking, compliance, and inspection readiness. Maintains CTMS and eTMF records, resolves data queries, prepares monitoring reports, and collaborates with investigators and cross-functional study teams to ensure participant safety, data quality, and timely study delivery.

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.