Regulatory Consultant

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. At Rho, we’re committed to you just as you’re committed to us. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve. We are currently hiring a Freelance Regulatory Consultant to join us in Moldova. This will be ad hoc work with approximately 1 - 2 hours work required per month. Responsibilities: Proofreading of translated label by checking the correctness of the translation, its spelling and grammar, text completeness, storage conditions; Regulatory review and local adaptation of translated label according to local regulatory requirements; Proofreading and regulatory review of label printouts; Approval of document by signing each page of document Regulatory consulting on various clinical trial related aspects (medicines and preferably devices/IVDs) in countries concerned; Interactions with Health Authorities, if applicable. Knowledge in local legislation and regulatory requirements in clinical trials field Degree in medicine, pharmacy, life science or related field will be considered as advantage Excellent knowledge of English language Strong organizational, communication and teamwork skills Accuracy and attention to details Computer literacy