Clinical Trial Associate

MCRA, an IQVIA business is seeking a strong In-House CRA to join our Clinical team. The In-House Clinical Research Associate will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial operations for the firm’s clientele.Position OverviewThe Clinical Trial Associate (CTA) supports the In-House Clinical Research Associate and clinical Trial Manager to ensure optimal management of essential documents with logistical and administrative tasks related to clinical trial start-up, execution and closing. The CTA supports regulatory document collection and tracking of monitoring visits and enrollment at the study-level. Responsible for completion of administrative tasks relating to implementing quality initiatives and the quality management system as applicable. This position is hybrid (2-3 days in office) out of our Washington, DC office.ResponsibilitiesSupport clinical project team by updating and maintaining clinical systems that track site compliance and performance within project timelines.Maintain Trial Master File (TMF) for multiple studies, including supporting periodic review of study files for accuracy and completeness.File, track and archive TMF documentation and reports.Create Investigator Site File (ISF) binders and patient binders for site use.Handle, distribute and track clinical trial supplies (non-IP) for site use.Support in-house CRA in documentation of all training sessions and/or meeting minutes as needed.Assist Clinical Affairs and Clinical Quality Assurance teams with preparation for internal quality audits and tracking of internal CAPAs (Corrective and Preventative Actions) as part of quality management reviews.Develop and maintain positive relationships both internal and external to projects, including clients, team members, and site personnel (PIs, Study coordinators, etc.)Required QualificationsBachelor’s degree in a scientific, management or related discipline.1-2 years of experience in an office environment.Proficiency with MS Office applications.Demonstrated professional oral and written communicationIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeThe potential base pay range for this role, when annualized, is $47,400.00 - $118,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.