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 requiring 1-2 hours of work 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.
• Collaborative team environment.
• Opportunity to innovate and develop a rewarding career.
• Work with a stable and thriving company.
• Respect for expertise and creative problem-solving.
• Focus on healthcare and clinical research.
• Commitment to employee well-being and growth.

Requirements

• Experience in regulatory review.
• Strong proofreading skills.
• Understanding of local regulatory requirements.
• Attention to detail.
• Ability to work independently.
• Good communication skills.
• Prior experience in clinical research is a plus.
• Fluency in the language of the translated documents.
• Ability to meet deadlines.
• Willingness to sign documents as required.

Benefits

• Flexible working hours.
• Opportunity to work with a respected team.
• Potential for long-term collaboration.
• Supportive work environment.
• Focus on personal and professional growth.