Clinical Trial Manager 2 (CTM 2) In partnership with Clinical Study Management, provide guidance and daily oversight for the successful in-house management of all aspects of international clinical trials, delivering high quality study data, on time and on budget. Develop and execute operational plans for the successful in-house implementation and management of oncology clinical trials. Collaborate with cross-functional teams, including data management, clinical scientists, regulatory and investigators, to ensure operational excellence and rapid delivery of high quality data. Manage all aspects of trial start-up activities, collaborating with other Clinical Operations functions (Site Engagement &

• Monitoring Excellence, and Supplier Relationship Management &

• Performance), to deliver efficient and effective site selection, feasibility assessments, and preparation of study-related documentation. Collaborate with other Clinical Operations functions (Site Engagement &

• Monitoring Excellence) to efficiently and effectively deliver study site initiation, training, and monitoring activities to ensure adherence to study protocols, regulatory requirements, and ICH-GCP guidelines. Collaborate with other Clinical Operations functions (Site Engagement &





• Monitoring Excellence) to develop and maintain strong relationships with investigators, study coordinators, and study site personnel to facilitate patient recruitment and retention. As required, collaborate with external vendors, including CROs, central laboratories, and imaging providers, to ensure their efficient and effective deliverables to the trial. and other clinical study management activities as assigned by Eikon Bachelor's or advanced degree in a relevant scientific discipline Oncology trial management experience preferred In-depth knowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP and FDA requirements, specific to oncology research Demonstrated experience in managing and executing clinical trials from start-up to closeout Strong project management skills, with the ability to effectively prioritize tasks, allocate resources, and manage study timelines and budgets Proficiency in using Veeva clinical trial management systems (CTMS) preferred Understanding of oncology therapeutic areas, including familiarity with oncology treatment modalities, disease progression, and related medical terminology.

📌 Clinical Trial Manager Consultant - II (Santiago)
🏢 ClinChoice
📍 Santiago