Teams at Rho (rhoworld.com)

Manages clinical study sites from feasibility and selection through initiation, routine monitoring, close-out, and file maintenance. Ensures data quality, regulatory and SOP compliance, timely study completion, and budget adherence. Responsibilities include Ethics Committee and Regulatory Authority submissions, site contract support, and country feasibility. Requires clinical research experience, strong communication in English and local languages, attention to quality, adaptability, a driver’s license, and travel availability.

Conduct site feasibility, selection, initiation, routine monitoring, close-out, and study file maintenance for assigned clinical studies. Ensure data quality, regulatory and SOP compliance, and timely, budget-conscious study completion. Prepare Ethics Committee and Regulatory Authority submissions, assist with site contract management, and communicate effectively with sponsors and sites. The role requires clinical research experience, English and local-language fluency, a driver license, and travel availability.

Manages clinical study sites across feasibility, selection, initiation, routine monitoring, close-out, and file maintenance. Ensures data quality, ICH-GCP and SOP compliance, regulatory adherence, and timely, budget-conscious study completion. Responsibilities include country and site feasibility, Ethics Committee and Regulatory Authority submissions, site contract assistance, and ongoing communication with sponsors and sites. Requires at least two years of on-site monitoring experience, relevant life sciences education, English and local-language fluency, a driver’s license, and travel availability.