Clinical Trial Coord

Senior Clinical Trial Coordinator oversees and coordinates trial activities (Central or Local) with responsibilities ranging from documenting and reviewing regulatory files to supporting cross-functional processes and study-level metrics. Key duties include coordinating trial activities per task matrix, performing file reviews (country/Internal/Investigator), maintaining study documentation and systems (eTMF, GoBalto), providing system and training support to the project team, scheduling meetings and capturing minutes, and ensuring tasks are completed on time and within budget. The role requires strong organizational skills, ability to work in a team or independently, proficiency with MS Office and clinical trial databases, knowledge of ICH GCP and regulatory requirements, and the ability to communicate effectively with stakeholders. Travel may be required and work may occur in office, laboratory, clinical, and home-office environments. Education includes a high/secondary school diploma or equivalent, with a Bachelor's degree preferred; previous relevant experience (4+ years) or an equivalent combination of education, training, and experience.