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, approximately 1 - 2 hours per month.
• Proofreading translated labels for correctness, spelling, and grammar.
• Regulatory review and local adaptation of translated labels.
• Approval of documents by signing each page.
• Consulting on clinical trial-related regulatory aspects.
• Interactions with health authorities as applicable.

Requirements

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

Benefits

• Opportunity to work in a stable and innovative environment.
• Collaboration with a talented and positive team.
• Freedom to think creatively and challenge norms.