Site Management Associate I PSI CRO AG Bogota, D.C., Capital District, Colombia Join our international team as a Site Management Associate I, supporting clinical research projects by streamlining communication, maintaining systems, and managing documents and information. Responsibilities include: Acting as the main contact between site personnel and CRAs, assisting with queries and EDC completion. Serving as the primary contact for vendors, study supplies, and access management. Ensuring pre-study testing of local site facilities is completed. Assisting monitors with documentation in CTMS and tracking site issues and actions. Managing clinical supplies' order, receipt, storage, distribution, return, and reconciliation. Handling regulatory submissions and notifications, staying updated on local regulations. Coordinating audits and inspections. Managing the TMF at site and country levels, including document filing and updates. Organizing and tracking training for site teams on vendor systems. Reviewing study documentation and translation statuses. Ensuring proper safety information flow with investigative sites. Qualifications: Degree in Life Sciences. Experience in administrative roles, preferably internationally. Experience as a CTA in CROs and in clinical research. Knowledge of local regulations. Proficiency in English and Spanish. Skillful in MS Office. Ability to work dynamically in a team and communicate effectively. Additional Information: Advance your career in clinical research by coordinating tasks and growing with the company. Details: Seniority level: Entry level Employment type: Full-time Job function: Administrative Industry: Pharmaceutical Manufacturing #J-18808-Ljbffr