Clinical Research Associate II / Senior CRA - Remote

Overview

Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

In Short

• Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)
• Participate in the site selection process with oversight from the Clinical Team Lead role
• Provide feedback to assist sites with resolution of detected deficiencies
• Contribute to the development and review of protocols and study materials
• Provide mentoring and training of junior clinical team members
• Develop and maintain effective working relationships with clinical sites
• Attend and present at meetings and conferences
• Participate in the RFP process and business development meetings
• Contribute to internal initiatives and standard operating procedures
• Perform both onsite & remote monitoring across multiple protocols

Requirements

• Experience in clinical monitoring and site management
• Knowledge of ICH Good Clinical Practices and FDA guidelines
• Ability to conduct site visits and assess compliance
• Strong communication and relationship-building skills
• Ability to travel up to 80%

Benefits

• Stable work environment with opportunities for career growth
• Collaborative and supportive team culture
• Financial rewards and job satisfaction