My client is an established Medical Device Research Organization who are looking for a Clinical Research Specialist to join their team. 12 Months Contract - 40 Hours per week - Remote, accepting applicants ideally local to Bogota Colombia. Brilliant remote opportunity for a clinical research professional who is looking to further their experience in medical device, site activation and on-site monitoring with a well-known and established organization. Responsibilities: Site Management & Coordination – Oversee clinical trial sites to ensure compliance with protocol requirements, regulatory guidelines, and study deliverables. Site Communication & Support – Serve as the primary point of contact for site staff, addressing queries, resolving issues, and ensuring sites have the necessary resources. Monitoring & Compliance – Ensure sites adhere to study timelines, meet key deliverables, and maintain high-quality data collection and documentation. Site Visits & Activation – Conduct on-site Site Initiation Visits (SIVs), support Site Activation, and perform remote site close-out activities. Audit & Inspection Readiness – Ensure sites maintain inspection-ready study documentation and assist in site audits as needed. Travel & On-Site Engagement – Travel to clinical sites as required to support study activities and maintain strong site relationships. Desired Background: 3+ years of Clinical Research Experience. Fluent English. Fluent Spanish. A life science bachelor’s degree. Knowledge of clinical trial regulations such as GCP/ICH, FDA requirements, and other regulations. If you are interested, get in touch with me ASAP by simply applying below. You can also send your most up-to-date CV directly to me, and I will reach out to you. [email protected] #J-18808-Ljbffr