.**Summarized Purpose**:Performs site management and other related activities on assigned project(s) in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and PPD SOPs. Reviews study data from various sources remotely. Develops collaborative relationships with investigational sites and other stakeholders as applicable. May contact study sites to collect study documentation, resolves issues and requests outstanding information. Detailed tasks and responsibilities assigned to RSM-Central or RSMLocal positions are outlined in the task matrix. Works proactively and almost independently, requiring mínimal supervision. Supports the line manager to mentor, train and contribute to the development of junior clinical team members.**Essential Functions**: According to the specific role (Central or Local) may coordinate, oversee and complete assigned trial activities as detailed on the task matrix, including but not limited to the following:- Develops and maintains a close and collaborative communication with the site staff. Actively discusses protocol conduction, enrollment rates and strategies, open issues, EDC completion and queries, as well as any other topic or indicator associated to project status and site performance.- Remotely reviews study logs as deemed necessary.- Conducts and documents site management calls/contacts according to the monitoring plan. Participates in investigator meetings. Investigates and followsup on centralized monitoring findings.- Provides refresher training, follows up on outstanding administrative needs (e.G., outstanding/updated regulatory documents), assists with regulatory reviews, as requested.- Reviews ad-hoc clinical listings review, tracks and trends violations and deviations, site status, enrollment, CRF status and SAE follow up.- Provides trial status tracking and progress update reports to study manager as required.- Participates in the investigator payment process, if applicable.- Liaises with internal staff to promptly collect documents, review data points and findings from EDC and file reviews, etc.- Assists in ensuring audit ready files and complying with CTMS and eTMF data stewardship. Contributes to company, client, and federal/local regulatory requirements/audit responses as needed.- Detailed task assignment and responsibilities are outlined on the task matrix, as well as any applicable protocol guidelines.**Education and Experience**:Bachelor's degree in life science-related field or an Associate's degree in Nursing with a current RN license. Internal applicants with current or previous CRA experience will be considered with or without the education requirements.Prior clinical research experience, 3+ years as well as knowledge of clinical monitoring through classwork/training that provides the required knowledge skills and abilities.Prefer individuals who aspire to advance into a CRA role
