Regulatory Consultant
Posted 516 days ago, which is unusual. The employer's own board was still carrying it when we last read it, just now.
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 2d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 516d ago
The date the source published, not the day we noticed it (2025-04-17). Last seen at its source just now.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
Moldova
The description states no restriction of its own. This is the source's own tag.
Carried by 1 source
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workable employer's own board first seen 11d ago · last seen just now
The listing
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