Medical Director, General Medicine - Remote

Overview

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do.

In Short

• Serve as Medical Advisor on assigned projects.
• Provide medical support to investigative sites and project staff for protocol-related issues.
• Perform review and clarification of trial-related Adverse Events (AEs) and coding.
• Perform medical case review of Serious Adverse Events (SAEs).
• Perform medical review of the protocol and high-profile documents.
• Serve as Scientific Advisor and provide guidance to Project Managers.
• Participate in the development of Medical Monitoring portion of client proposals.
• Support Business Development activities with medical/scientific input.
• Support Feasibility activities as required.

Requirements

• Expertise in medical, clinical, and scientific advisory.
• Experience in clinical trial design and conduct.
• Knowledge of regulatory requirements.
• Ability to review clinical documentation and provide insights.
• Strong communication and collaboration skills.
• Experience in business development and proposal writing.

Benefits

• Opportunity for career growth and stability.
• Supportive community and collaborative environment.
• Engagement with innovative projects.
• Competitive financial rewards.