Coordinate clinical trial operations at Pratia’s Plovdiv research site, supporting patients and study teams. Maintain study records and databases while helping ensure work follows clinical research procedures.
GermaniaHibridNormă întreagăNivel mediuSeniorLimbă Obligatorie: germanăLimbă Obligatorie: englezăCreanțe comercialeManage clinical-trial billing and study budgets for Pratia Germany. Coordinate financial administration with sponsors, trial sites, and internal teams.
Lead endpoint adjudication and clinical trial data coordination for Humaneva Group in India. Maintain data quality, regulatory compliance, documentation, and collaboration across vendors and study stakeholders.
Lead Humaneva Group’s platform and data strategy for clinical research infrastructure and business data operations. Guide architecture, reliability, modernization, governance, compliance, and engineering team development.
Support clinical trial administration in Varna by organizing documentation, coordinating study activities, and assisting Pratia’s clinical research team. Maintain accurate records and help uphold quality and compliance standards.
