Sr Clinical Data Associate

Clinical Data Associate II responsible for advanced data cleaning per Good Clinical Practices and SOPs/WPDs, to assess safety and efficacy of investigational products and/or medical devices. Primary duties include identifying and resolving data discrepancies, updating the data management database, generating and resolving data clarifications and queries, reviewing data listings for accuracy, producing project-specific status reports for CDM management and clients, and performing data management activities such as Serious Adverse Event and Third Party Vendor reconciliations and Data Listing reviews. Requires a high school diploma or equivalent with substantial relevant experience (at least 6 years), proficiency with regulatory guidelines and client expectations, strong attention to detail, excellent written and verbal communication in English, ability to work under moderate supervision, and ability to maintain confidentiality. Travel occasionally to site locations may be required; office/clinical environment.