Qualifications A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required. A minimum of 3 years of clinical trial monitoring experience. Other relevant experiences and skills may be considered by the hiring manager when considering the candidates eligibility. Strong understanding of GCP, company SOPs, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines. Strong IT Skills In Appropriate Software And Company Systems. Willingness to travel up to 75% with occasional overnight stay away from home. Proficient in speaking and writing the country language and English. Good written and oral communication. Responsibilities Acts as primary local company contact for assigned sites for specific trials. May participate in site feasibility and/or pre-trial site assessment visits Attends/participates in investigator meetings as needed. Responsible for executing activit...