Freelance Clinical Research Associate

🔥 8 minutes ago

🇫🇷 France – Remote

⏳ Contract/Temporary

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Rho

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1984

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Rho is a financial technology company that provides integrated banking solutions for businesses, combining modern banking with cash management and expense tracking. Their platform focuses on streamlining financial operations and offering a user-friendly interface for better control of company finances.

📋 Description

• Manage all aspects of study site management, including site selection, initiation, routine monitoring, close-out, and maintenance of study files • Ensure data quality and integrity, compliance with relevant SOPs and regulatory requirements, and study completion on time and within budget • Perform site administration and monitoring for assigned clinical studies according to Dokumeds and Sponsor SOPs, legal requirements, and ICH-GCP Guidelines • Conduct country and site feasibility • Conduct site initiation, routine monitoring, and close-out visits • Prepare and submit documentation to Ethics Committees and Regulatory Authorities • Assist with site contract management

🎯 Requirements

• University degree in medicine, pharmacy, nursing or life science • At least 2 years of previous on-site monitoring experience in CRO or Pharma company • Previous freelancing experience will be considered as an advantage • Previous experience in preparation and submissions to Ethics Committees / Regulatory Authorities • Strong written, verbal and presentation skills • Fluency in both English and local languages • Attention to detail and understanding of high-quality scientific standards • Honesty, integrity, loyalty, accountability, mutual trust, and strong team spirit • Critical thinking and ability to craft novel, practical solutions • Ability to change quickly, anticipate and respond to changes, and manage risk • Driver license and ability to travel • CV submitted in English

🏖️ Benefits

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