Clinical Research Assistant

Clinical Research AssistantThe primary function in this position will be to provide departmental administrative support in the area of Clinical Affairs, including:Perform quality checks, uploads and tracking of required regulatory documents to populate the electronic Trial Master File (TMF) for designated studies. Generate reports of missing documents and upcoming expiration dates. Communicate with sites and/or study team to obtain required documents. Ensure the TMF is audit-ready in support of regulatory filings.Obtain safety-related source documents and images from clinical sites in preparation for Clinical Event Committee and Data Safety Monitoring Board meeting packages. Work with translation vendors as needed.Track device inventory and prepare shipments to sites, ensuring device integrity is maintained (i.e., temperature control and expiration dates). Process returned/expired devices.Assist with the distribution and tracking of clinical study supplies to Contract Research Organizations (CROs) and clinical centers (e.g. study binders, case report form worksheets, study devices and misc. materials)Interface with CROs to obtain study-related documentation and follow up on action itemsAssist with site invoicing and payment trackingAssist with organization and filing of study related materialsAssist in the organization and execution of Investigator meetingsProvide general administrative support as neededUndergraduate degree2-3 years of relevant clinical trial experienceMinimum of 1-2 years of clinical study electronic Trial Master File experienceProficient with basic computer programs such as Microsoft Word, Excel PowerPoint and Adobe AcrobatDetail oriented in document review and error checkingEffective communication skillsMinimum of 1-2 years of Sponsor or CRO experienceWorking knowledge of CDISC TMF Reference ModelWhile performing the duties of this job, the employee is frequently required to sit or stand for prolonged periods of time, frequently in front of a computer.