Teams at Parexel

Lead global regulatory labeling strategy and governance for pharmaceuticals, managing core labeling documents (CDS, USPI, SmPC), committee leadership, regulatory submissions, health authority negotiations, advertising/artwork review, and cross-functional implementation to ensure compliant, high-quality labeling across international markets.

Lead data quality and data management for oncology studies, overseeing DM teams, vendor/CRO management, and compliance with CDISC/ICH-GCP. Develop risk management, integrate and surveil multi-source data, advise stakeholders on data collection and standards, produce metrics and dashboards, manage project resourcing and finances, review contracts, and deliver training to ensure high-quality, regulatory-compliant clinical and real-world data.

The Senior Clinical Research Associate manages clinical trial sites, ensures adherence to regulations, oversees study conduct, and resolves issues while safeguarding patient safety.