• Works on multiple trials within the Cross Therapeutic areas - Start up focus • Collaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements. • Perform Site Qualification Visits (SQVs) to assess the eligibility of sites for participation in specific clinical studies. • Build strong relationships with site personnel to facilitate a smooth onboarding process. • Ensure that all activities adhere to ICH-GCP guidelines, local regulatory standards, and internal Standard Operating Procedures (SOPs). • Coordinate with the country operations team to collect essential documents (such as regulatory approvals and contracts) to enable timely site activation. • Act as the main point of contact for sites, study teams, and external stakeholders throughout the start-up process. • Work closely with the country operations team to manage investigator contracts, regulatory documents, and site-specific start-up activities. • Provide regular status updates to both internal and external stakeholders, ensuring alignment with important project milestones. • Monitor, report on, and analyze key performance indicators (KPIs) related to site selection and start-up timelines. • Proactively identify and address any issues that may delay study initiation or affect trial deliverables. • Maintain precise documentation to ensure readiness for inspections. • Support sites during the activation phase until they achieve “Green Light” status for site opening. • Facilitate coordination with site staff to ensure all pre-study requirements, including contracts, budgets, and essential documentation, are met. • Possibly assist in audit and inspection preparations to guarantee compliance with regulatory and ethical standards.