Freelance Regulatory Consultant (Ad Hoc, 1‑2 hrs/month)

About the role

Rho is seeking a freelance Regulatory Consultant to support its clinical research activities in Moldova on an ad‑hoc basis. The role involves a few hours each month, allowing you to apply your regulatory expertise while enjoying flexibility.

Key responsibilities

• Proofread translated product labels, checking spelling, grammar, completeness and storage conditions.
• Conduct regulatory review and adapt translated labels to meet local regulatory requirements.
• Proofread and review label printouts for compliance.
• Approve documents by signing each page.
• Provide regulatory consulting on clinical‑trial‑related matters for medicines and, preferably, devices/IVDs.
• Interact with Health Authorities when required.

Required profile

• Knowledge of local legislation and regulatory requirements in the clinical‑trial field.
• Degree in medicine, pharmacy, life sciences or a related discipline (advantageous).
• Excellent command of English.
• Strong organizational, communication and teamwork abilities.
• High accuracy and attention to detail.

Required skills

• Computer literacy.

What we offer

• Opportunity to work with a collaborative, innovative CRO.
• Flexible, part‑time freelance arrangement (1‑2 hours per month).
• Exposure to international regulatory environments.