Description
Alkeus Pharmaceuticals is hiring an eTMF Associate to support the management, quality, completeness, and inspection readiness of electronic Trial Master Files across clinical development programs. The role collaborates with clinical study teams, CROs, vendors, and regulatory stakeholders to file and track documents, monitor TMF quality metrics, support inspections and CAPA activities, coordinate document collection, and improve TMF processes. The position requires a bachelor’s degree or an associate degree plus relevant experience, 1–3 years of clinical research, document management, quality, or clinical operations experience, and the ability to travel globally up to 20% of the time. The base salary is $55,000–$75,000, with a discretionary bonus of up to 5% of base salary and medical, dental, and vision insurance benefits.
