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The Clinical Supply Specialist manages clinical supply execution including planning, shipment oversight, inventory tracking, and coordination with stakeholders and vendors across EU and US.

Lead cross-functional teams to manage complex clinical trials across various health sectors while ensuring compliance with GCP and regulatory standards.

Lead and manage clinical projects, ensuring compliance with regulations and overseeing trial operations, specifically in hematology and oncology.

The Business Development Director will generate leads, assess opportunities, build relationships with clients, and meet revenue targets for a CRO.

The Business Development Director will sell CRO services, generate leads, assess opportunities, and develop and grow client accounts, focusing on relationship management and exceeding revenue targets.

The Business Development Director will identify and pursue new business opportunities, manage client relationships, develop account plans, and exceed revenue targets for CRO services.

The Principal Statistical Programmer Consultant leads programming efforts for clinical studies, ensuring quality deliverables and compliance with industry standards, while collaborating with study teams and managing concurrent project activities.

The Statistical Programmer/Analyst III analyzes data, develops SAS programs following CDISC standards, creates datasets, and supports regulatory submissions. Responsibilities include data analysis, programming, and communication with statisticians.

The Principal Data Scientist Consultant will develop and maintain clinical datasets using R, ensure CDISC compliance, generate reports, and contribute to internal tools while collaborating with clinical teams.

The role involves completing a clinical programming training program, producing statistical analysis with SAS/R, ensuring compliance to SOPs, and developing SAS programs for study data analysis.