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We are seeking an experienced Clinical Trials Manager to lead the execution of clinical studies within assigned therapeutic areas. This role is responsible for driving study operations, managing cross-functional teams, and ensuring successful delivery of clinical trials in compliance with regulatory standards. This position requires a strong sponsor-side project management background and the ability to drive CRO and vendor performance to meet critical timelines, quality expectations, and budget targets.
Job Responsibility:
Lead end-to-end clinical trial management activities across assigned studies
Drive CRO and vendor performance, ensuring accountability, quality, and adherence to timelines
Oversee vendor relationships, including audits and performance evaluations
Develop and contribute to key regulatory documents (protocols, investigator brochures, clinical study reports)
Manage study timelines, milestones, and risk mitigation strategies
Coordinate investigator meetings and cross-functional study execution