Rho is a full-service Contract Research Organization (CRO) that combines innovation and scientific rigor to maximize results in every phase of clinical research. With a global team of experts, Rho ensures consistent and efficient trials, offering compr...
Enter your details and select criteria for the jobs you want to receive.
Rho is hiring a remote Associate Clinical Team Lead to support clinical operations oversight, CRA leadership, compliance, and stakeholder coordination across clinical research projects, with occasional travel.
Rho is seeking a Director/Senior Director of Project Delivery with respiratory clinical research expertise to oversee portfolios from proposal development through execution, ensuring operational excellence, financial performance, risk management, and strong client partnerships.
Rho is seeking a Director/Senior Director of Project Delivery with respiratory expertise to provide strategic oversight of clinical research portfolios from proposal development through execution while driving operational, financial, and client success.
Rho is hiring a Clinical Data Associate to support clinical data management and programming work within its clinical research team.
Rho is hiring an Accounts Payable Specialist in Warsaw, Poland to process supplier invoices and employee expenses across multi-entity, multi-currency operations while ensuring accurate, compliant, and timely payment processing.
Rho is hiring a Clinical Research Associate II or Senior Clinical Research Associate to support pain study monitoring and site management across multiple clinical protocols.
Rho is seeking a remote Study Start Up Lead to oversee site activation and startup activities across multiple countries, ensuring timely regulatory, operational, and cross-functional execution for clinical trials.
Rho is hiring a remote Clinical Team Lead to manage clinical operations for assigned CRO projects, overseeing CRA and site performance, compliance, and cross-functional study execution.
Freelance Regulatory Consultant at Rho in Moldova providing ad hoc regulatory review and local adaptation of clinical trial labeling and consulting to ensure compliance with local requirements (approximately 1–2 hours/month).
