Responsibilities
• Leads Local Study Team(s) at country level to deliver components of clinical studies
• Ensures study commitments within the country and timely data delivery
• Coordinates site selection process and conducts Site Qualification Visits
• Manages monitoring activities from site activation to study closure
• Organizes Local Study Team meetings and communicates with stakeholders
Requirements
• Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields
• Good knowledge of international guidelines ICH GCP as well as relevant local regulations
• Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
• Fluent in written and spoken English and local language(s) required
• Excellent project management skills