Freelance Regional Clinical Trial Coordinator (not posted, see req 2024-2700) at Rho

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.

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 Regional Clinical Trial Coordinator to join our team! This can be home-based in Poland, Estonia, Lithuania, or Latvia! 

Our Clinical Operations team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

Technical and administrative support of international Studies:

• Maintenance of Trial Master File (TMF) and periodical quality checks of TMF to ensure accuracy, completeness
• Maintenance of Clinical Trial Management System and other applicable systems/ trackings for Study specific activities - set up of share point, public drives and other systems
• Support in preparation of Investigator Site Files
• Timely transfer of Study documents (original and/or scanned copies) to the assigned Party, follow up with other study team members
• Support in Study documents translation and translation verification
• Support in preparation of critical documents package for submission to Competent Authorities and Ethics Committee
• Meetings preparation, drafting telephone conference and meeting minutes
• Other technical and administrative support within the organizational/ project structure as applicable

• Degree in medicine, pharmacy, life science or related field will be considered as advantage
• Previous experience in Clinical Trial Assistant or similar role for at least 1 year
• Excellent knowledge of English languages
• Strong organizational, communication and teamwork skills
• Accuracy and attention to details
• Computer literacy

We offer:

• Competitive salary
• Opportunity to learn and grow professionally in Clinical Research field
• A job with daily exciting challenges in a highly qualified and international team
• Employee-friendly work environment

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