The Scientific Report Associate is responsible for generating, templating, and formatting preliminary and final Clinical Study Reports. This role involves building appendices and ensuring documents meet client specifications regarding styles, tables, and formatting.
The Biostatistician is responsible for developing statistical analysis plans and performing statistical analyses using SAS for clinical research projects. They will also coordinate data collection methods, generate randomization schedules, and prepare comprehensive reports for internal and external stakeholders.
The Director will drive strategic growth for Celerion's Bioanalytical Services by acquiring new clients and programs within biologics and biomarkers. They will serve as a technical commercial leader, building relationships with scientific and executive decision-makers to expand the company's presence in patient-based clinical development.
The TMF Representative is responsible for the preparation, maintenance, and indexing of Trial Master Files to ensure compliance with study protocols and regulatory requirements. They will also act as a point of contact for sponsors, project managers, and study sites to facilitate effective communication and study documentation.
