Job Description
📋 Description Independently perform site monitoring activities onsite/remote; document per SOPs & study Collaborate with site staff to ensure data is accurate and compliant Monitor data queries, resolve issues, escalate as needed Coordinate shipment of clinical supplies (IP, lab supplies, ePROs, docs) Train site staff on protocol, systems, ICH-GCP Participate in progress meetings and Investigator’s meetings 🎯 Requirements College diploma/degree with 4-6 years of related experience Fluent in English, Dutch and French Proficient with EDC (Medidata Rave, Oracle InForm), IRT, eTMF, CTMS, Microsoft Office Willing to travel up to 40-60%; strong communication & organizational skills Knowledge of ICH-GCP and local regulatory requirements 🎁 Benefits Sign-On Bonus: €3,000 Annual Bonus target 8% of salary Monthly mobile stipend (€40) and other allowances Expense reimbursement up to €500 for office items Mileage reimbursement for travel
