Rwe Site Managers

Job OverviewEssential Functions- Oversee the work of assigned site management staff, providing advice and guidance to help achieve quality deliverables on site.- Assist with the development of Site Recruitment, SPS Operations and SPS Risk Management Plans.- Ensure that clinical monitoring tasks are conducted in accordance with protocol, process, quality standards and expectations, per contract.- Collaborate with other functional groups within the company such as data management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.- Manage and follow study activities through ongoing tracking and review of study progress. Report progress to appropriate SPS management and project management leaders.- Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.- Provide input and updates to the Clinical Project Manager regarding the monitoring status and CRA team progress and deliverables.- Act as the first line of escalation for site management questions and issues for their assigned projects.- Conduct co-monitoring and/or assessment visits to ensure the study is being conducted in accordance with the protocol, SOPs, GCP and applicable regulatory requirements.- May act as site visit report reviewer.- May conduct monitoring and/or assessment visits as needed to ensure the study is being conducted in accordance with the protocol, SOPs, GCP and applicable regulatory requirements.**Qualifications**:- Bachelor's Degree in a health care or other scientific discipline- 1 - 3 years of clinical research experience (monitoring, regulatory, CTA)- Advanced English level