Description
To streamline communication across cross-functional stakeholders throughout trial lifecycles, the full-time remote Senior Clinical Trial Manager will serve as the primary point of contact for trial sites, ensuring compliance, managing site relationships, and overseeing recruitment strategies in Solid Tumor Oncology studies.Key responsibilitiesManage relationships with trial sites, facilitating communication and issue resolution throughout the trial lifecycleEnsure recruitment targets are met by leading local team activities and contributing to site selection and feasibility assessmentsMaintain trial compliance and data quality by managing trial management systems and initiating corrective actions as necessaryRequired qualificationsBA/BS degree in a health or science-related field3 - 5+ years of end-to-end trial management experience, with a focus on Solid Tumor OncologyStrong knowledge of ICH-GCP, local laws, and regulations related to clinical trialsProficient in relevant software and systems, with strong IT skillsFluent in the country language and English, with good written and oral communication skills
Description
To streamline communication across cross-functional stakeholders throughout trial lifecycles, the full-time remote Senior Clinical Trial Manager will serve as the primary point of contact for trial sites, ensuring compliance, managing site relationships, and overseeing recruitment strategies in Solid Tumor Oncology studies.Key responsibilitiesManage relationships with trial sites, facilitating communication and issue resolution throughout the trial lifecycleEnsure recruitment targets are met by leading local team activities and contributing to site selection and feasibility assessmentsMaintain trial compliance and data quality by managing trial management systems and initiating corrective actions as necessaryRequired qualificationsBA/BS degree in a health or science-related field3 - 5+ years of end-to-end trial management experience, with a focus on Solid Tumor OncologyStrong knowledge of ICH-GCP, local laws, and regulations related to clinical trialsProficient in relevant software and systems, with strong IT skillsFluent in the country language and English, with good written and oral communication skills
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