Regional Clinical Research Associate (CRA)

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.Are you looking to be part of a growing company that works on challenging programs of a global nature; a company known for it's expertise and quality services? SRA International's global drug development unit, (formerly Constella Group) 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 program management. We are seeking Regional Clinical Research Associates (CRA) to join our monitoring team. Our CRAs will monitor Phase I - IV drug and device studies, across all therapeutic areas. Areas of expertise include, but are not limited to: oncology, diabetes, HIV/AIDs, sexual dysfunction, vaccines, and CNS. Opportunities available for full-time or part time employees both locally and regionally based. Travel: 55 - 70%. Essential Functions: Performs investigator recruitment, pre-study, site initiation, interim monitoring, and close-out visits Establishs and maintains relationships with sponsors, study sites and team members to ensure professional, timely, and ongoing communication and oversight for each project Comprehends, follows and implements GCP guidelines and 21 CFR to ensure that clinical monitoring services are performed accurately and appropriately within federal guidelines Assists with training and mentoring of other CRAs Works on multiple clinical trials of various therapeutic areas. Typically CRAs work on only 2 - 3 clinical trials at once. **We are currently only hiring experienced CRAs. Please do not apply unless you have previous CRA / clinical field monitoring experience. Requires 2 - 8 years of direct experience monitoring clinical research trials in the field. Strongly prefer experience monitoring complex studies, such as in patient, oncology, transplant, HIV/AIDS, Sepsis, etc Electronic Data Capture (EDC) experience strongly preferred Previous study coordinator or nursing experience strongly preferred BS, LPN, or RN degree preferred Ability to work independently and as a member of the team Attention to quality and detail Excellent written and communication skillsTo learn more about SRA International, go to www.sra.com.SRA International is an Equal Opportunity Employer. Company:SRA International, Inc. Reference Code:16812BR