Clinical Trial Manager

Role Overview: This position involves managing and supporting the planning, setup, and execution of global clinical trials in accordance with quality standards and regulatory requirements. The role includes overseeing trial documentation, collaborating with CROs and internal teams for site feasibility and management, and ensuring service provider performance aligns with study expectations. Key Responsibilities Support trial activities, including oversight, documentation, and inspection readiness.Coordinate with external and internal stakeholders for site selection, activation, and management.Monitor service providers, track deliverables, and ensure quality and timelines.Identify and mitigate risks, manage protocol deviations, and address trial-level issues.Assist in data review, performance tracking, and reporting.Foster collaboration within a global, matrixed team environment. Qualifications & Skills Bachelor’s degree in life sciences or related field; Master’s preferred.At least 5 years of experience in clinical trial management, with knowledge of ICH/GCP regulations.Experience managing global, multi-center trials within complex organizations.Strong project management, communication, and interpersonal skills.Experience in oncology or specific therapeutic areas is highly desirable.