Teams at Worldwide Clinical Trials

Lead Quality Assurance activities across global studies, ensuring compliance with regulations. Provide GCP consultancy and manage quality issues. Participate in risk management and audits.

Lead statistical support for clinical trials: design consultation, write and review SAPs, develop and validate SAS programs and CDISC datasets (SDTM/ADaM), produce tables/figures/listings, support reporting, QA, bids, and process improvements while ensuring regulatory compliance.

Lead business development for Phase II-IV CRO services across assigned UK/Europe territory. Generate new client relationships, respond to RFPs, drive revenue targets, develop account strategies, attend trade shows, and present to clients and senior management to secure and grow contracts.