Clinical data Spec- Coordinator
<p><b>Clinical Data Specialist β Coordinator</b></p><p>π <b>Location: Costa Rica (candidates must be based in Costa Rica)</b><br>𧬠Department: Clinical Data Management</p><p><b>Advance clinical research through data precision</b></p><p>We are looking for a detail-oriented and collaborative <b>Clinical Data Specialist β Coordinator</b> to join our growing Clinical Data Management team.</p><p>In this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide.</p><div></div><p><b>What Youβll Do</b></p><ul><li>Support the acquisition, review, and integration of external clinical trial data throughout the study lifecycle</li><li>Coordinate with internal teams and external vendors to ensure accurate and timely data delivery</li><li>Perform data quality checks and assist in resolving discrepancies</li><li>Contribute to study deliverables under the guidance of experienced data leads</li><li>Participate in study-related activities, including meetings and task coordination</li><li>Help prioritize tasks, manage timelines, and escalate issues when needed</li><li>Work across multiple studies with diverse data sources and therapeutic areas</li></ul><div></div><p><b>What You Bring</b></p><ul><li>Bachelorβs degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)</li><li>Approximately 1+ year of experience in clinical research or drug development</li><li>Basic understanding of clinical trials, ICH-GCP, and data quality principles</li><li>Familiarity or interest in clinical data standards (e.g., CDISC, SDTM, ADaM)</li><li>Strong attention to detail and problem-solving skills</li><li>Effective communication and collaboration abilities</li><li>Ability to manage multiple priorities in a dynamic environment</li><li>Proficiency in Microsoft Office tools</li></ul><div></div><p><b>Why Join Us?</b></p><ul><li>π Work on global clinical trials across diverse therapeutic areas</li><li>π Build expertise in clinical data and external data integration</li><li>π€ Collaborate with cross-functional and international teams</li><li>π Grow your career in a supportive and structured environment</li></ul><div></div><p><b>Important Requirement</b></p><p>β <b>Candidates must be currently based in Costa Rica</b><br>Β </p><p><b>Who You Are</b></p><p>You are detail-driven, proactive, and eager to build a career in Clinical Data Management. You thrive in a collaborative environment, enjoy solving problems, and are motivated by contributing to high-quality clinical research.</p><div><p></p></div><p></p><p><span>Learn more about our </span><a href="https://careers.fortrea.com/us/en/eeo-and-accommodations" target="_blank" rel="noopener noreferrer">EEO & Accommodations request here</a><span>.</span></p>