Regulatory Consultant

Description

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.

Requirements

• 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