Inhouse Clinical Research Associate

W2 indefinite contract 40hrs a week West Coast Candidates only In-House Clinical Research Associate (CRA) Seeking a proactive, detail-oriented In-House CRA to support early- and late-phase clinical trials in a fast-paced biotech setting. This role is central to study operations, vendor oversight, and ensuring quality and compliance from start-up through close-out. Key Responsibilities Manage site feasibility, selection, start-up, and close-out documentation. Maintain CTMS and study trackers to monitor site activation, enrollment, and performance metrics. Support remote site monitoring, review reports and ICFs, and track resolution of issues with field CRAs. Serve as point of contact for select vendors, review reports for accuracy, and track performance. Maintain eTMF to inspection readiness and support cross-functional study communication. Qualifications Bachelor's in life sciences (or related field) preferred; Associate's with relevant experience considered. 1–3 years' clinical research experience, ideally in biotech or sponsor settings. Knowledge of GCP, ICH, and regulatory requirements. Proficiency with Veeva Vault, EDC, IRT, CTMS, and Microsoft Office. Strong organizational, communication, and problem-solving skills. Willingness to travel domestically up to 20%.