Site Identification Analyst II

Role: Site Identification Analyst II supporting clinical operations within the Clinical Monitoring, Site Management, and SSU team. Primary objectives include managing site outreach, supporting site identification activities, and ensuring timely data management in clinical trials. Responsibilities involve maintaining relationships with internal/external stakeholders, tracking site activities via CTMS, updating investigator databases, and overseeing site capability assessments through SRQ reviews. Requirements: undergraduate degree in sciences or related field; 3+ years in data management or clinical operations within pharma, biotech, or medtech; 2+ years supporting CTMS systems; experience in clinical trial support, site identification, or site partnership management. Skills: strong analytical/problem-solving abilities; proficient in EDC and CTMS platforms. Preferred: experience with clinical trial startup processes and site selection. High-Value specifics include focus on clinical trial site management, supporting biotech/medtech/pharma studies, and working with CTMS and database systems. Collaboration and reporting are integral, with a focus on maintaining project timelines and quality data. Work setup includes supporting global clinical trial operations with a remote or hybrid modality.