Freelance Regulatory Consultant - 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

• Freelance position with ad hoc work in Austria.
• Approximately 1 - 2 hours of work required per month.
• Responsibilities include proofreading and regulatory review of translated labels.
• Local adaptation of labels according to regulatory requirements.
• Approval of documents by signing each page.
• Consulting on clinical trial-related aspects.
• Interactions with Health Authorities as needed.
• Work within a collaborative and innovative environment.
• Opportunity to experience a stable company.
• Celebration and respect for expertise.

Requirements

• Experience in regulatory consulting.
• Strong proofreading skills.
• Knowledge of clinical trials and regulatory requirements.
• Ability to interact with health authorities.

Benefits

• Flexible work schedule.
• Opportunity to work in a supportive environment.
• Potential for long-term collaboration.