Job Number: 233642Clinical Study Associate Level 1-6462Softworld is seeking a full-time complementary worker to focus on file management of Investigator Sponsored Research (ISR) Program to include, file clean-up, filing documents, archiving and any other tasks needed by the Operation Team.Responsibilities include: Review current study files for quality and accuracy and align data across systems. Organize current publications and align ViSiONS and Datavision database. Review and maintain study/site information in ViiV database systems (i.e., ViSiONS, eTrack, Datavision, GCMS, PIER, Veeva vault). Coordinate meetings with key stakeholders to obtain missing information.Minimum Requirements: High School Diploma plus two years experience in pharmaceutical industry or health related field Ability to work effectively within interdisciplinary teams Ability to effectively handle competing priorities Computer proficiency in a variety of databases and software applications Ability to manage projects and assignments with minimal supervisionIdeal Candidate Skills: Advanced proficiency in Microsoft Excel Experience in PubMed and Clinicaltrials.gov Experience with CTMS, eTMF (i.e., Veeva Vault) Bachelor's degree in life sciences Knowledge of study processes and procedures, including FDA regulations THIRD PARTY AGENCIES, SUBCONTRACTORS, AND RECRUITERS NEED NOT APPLY. Applicants received from firms will not be considered. Subcontracting is not available for this position.