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

• Ad hoc work with approximately 1 - 2 hours work required per month.
• Proofreading of translated labels for correctness, spelling, grammar, and completeness.
• Regulatory review and local adaptation of translated labels according to local regulatory requirements.
• Approval of documents by signing each page.
• Regulatory consulting on clinical trial aspects related to medicines and devices/IVDs.
• Interactions with Health Authorities, if applicable.

Requirements

• Experience in regulatory consulting.
• Strong proofreading skills.
• Knowledge of local regulatory requirements in Kazakhstan.
• Ability to interact with Health Authorities.

Benefits

• Opportunity to work with a collaborative team.
• Flexible work schedule.
• Stability in a thriving company.
• Environment that fosters innovation and creativity.