Teams at Bristol Myers Squibb

Leads clinical data management across multiple pharmaceutical and biotech clinical trials. Oversees data management personnel, CROs, vendors, timelines, quality, data integrity, clinical systems, and regulatory compliance. Reviews data listings and visualizations for quality and trend analysis, manages third-party laboratory data interactions, participates in cross-functional meetings, and contributes to SOP development. Requires at least six years of data management experience and may require 10% travel.

Provides strategic and operational leadership for global clinical trials, overseeing study teams, CROs, vendors, budgets, timelines, quality, risk mitigation, and regulatory compliance. Leads trial planning, execution, closeout, inspection readiness, and cross-functional decision-making. Contributes to clinical development plans and protocol design, drives process improvements, and supports governance activities. The role requires pharmaceutical or biotech clinical operations experience, including oncology trials, with up to 20% travel.

Leads Phase I–III clinical trial planning, execution, and closeout. Oversees CROs, vendors, budgets, timelines, site activation, enrollment, data quality, risk mitigation, and regulatory compliance. Coordinates cross-functional study teams, monitors performance, escalates issues, and supports operational strategy. Requires 5–7 years of clinical operations experience in biotech, pharma, or CRO settings, with up to 20% travel.