Senior Clinical Research Manager

Role: Senior Clinical Research Manager overseeing clinical monitoring activities and CRA team performance in cancer-related clinical trials. Objectives include ensuring compliance with ICH-GCP, local regulations, and maintaining high-quality trial execution. Responsibilities encompass resource allocation, monitoring quality, site relationship management, regulatory compliance, and supporting study milestones. The role involves managing CRA performance, conducting assessments, supporting audits, and optimizing processes. It also includes mentoring junior staff, leading strategic initiatives, and supporting team development. Qualifications: minimum 7 years’ industry experience in pharma, CRO, or related field; 4+ years in people or project management; bachelor's degree in a scientific/healthcare discipline (advanced degrees preferred). Skills required include thorough understanding of drug development, GxP, monitoring, trial execution, and oncology experience highly recommended. Proficiency in Microsoft Office and fluency in English are essential. High-value biopharma specifics: oncology focus, clinical trial oversight, regulatory compliance, and team leadership in a global setting. Work setup involves travel as needed; location flexibility not specified.