Project Assistant

SRA International, a dynamic 28 year industry leader whose focus is on providing technology and strategic consulting services to clients in the National Security, Civil Government and Public Health sectors is looking for talented individuals to join our team. Named by FORTUNE Magazine as one of the "100 Best Companies to Work For" 8 years in a row speaks for itself, not to mention our steady financial performance and growth. Our success is attributed to the core values we have stressed since our inception: an ethic of honesty and service; quality work and customer satisfaction; and caring about our people. If you’re looking to make a difference and work on "Missions that Matter" we encourage you to make SRA your employer of choice.SRA International's global drug development unit assists both pharmaceutical and biotechnology clients in all areas of drug development. These areas include: Phase I - IV clinical trials (including clinical monitoring, trials management, data management, statistics and SAS programming); regulatory affairs and product development consulting; quality assurance; medical writing; Pharmacovigilance; and programme management. We are seeking a Project Assistant to join our clinical operations department within the global drug development unit. Clinical Project Assistants are an integral part of our clinical project teams. Key responsibilities of our Project Assistants include assisting clinical project teams with tracking investigator recruitment, enrollment, monitoring visits, etc; collecting regulatory documents; mailing essential documents to study sites and other team members; taking meeting minutes and distributing to the team; and other support activities as needed. Our Clinical Project Assistants are typically dedicated to 1 - 2 projects and intregrally involved with the project team. Position is full time and based in our Durham office.Essential Functions: Develop and maintain spreadsheets and Activity Tracking database to track information to ensure up-to-date project information is available for review, analysis and reporting Assist in all project start-up activities including setting up and managing project files and distributing accurate project information packets to sites Compose correspondence and memoranda, proofread final communications, coordinate mass mailings, input, copy, and circulate reports Establish and maintain relationships with sponsors, study sites and team members to ensure professional, timely, and ongoing communication and documentation for each project Attend project and corporate meetings as necessary and record and distribute meeting minutes when applicable Assist in compiling and preparing project related materials, e.g., visual materials, study newsletter, etc. Distribute supply supplies to sites as neededRequired Experience: " AA/AS degree and 4+ years of professional administrative support " At least 1 year in direct support of clinical studies strongly preferred " Excellent computer knowledge and skills, e.g., Word, Excel, mass fax, and PowerPoint and proficient in researching topics on the Internet " Excellent organizational and time management skills " Good communication skills, both written and verbal " Good attention to detailSRA offers a competitive benefits package.To learn more about SRA International, go to www.sra.com.SRA International is an Equal Opportunity Employer. Company:SRA International, Inc. Reference Code:17580BR