Clinical Trial Manager – Contract

Job not on LinkedIn

🔥 4 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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Resilience

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2020

🏭 Manufacturing

🏥 Healthcare

📦 Logistics

Manufacturing • Healthcare • Logistics

Resilience is a leading biomanufacturing innovation company focused on the development of novel medicines. Specializing in the manufacturing of complex medicines such as cell and gene therapies, Resilience partners with small and mid-sized biotech firms to provide customized solutions that leverage cutting-edge technologies and scientific advancement. Their approach includes high-tech, end-to-end drug substance and drug product manufacturing capabilities aimed at ensuring rapid, safe, and scalable production. Resilience operates primarily in North America, with expertise in delivering regulatory-compliant solutions across global markets, enhancing the reliability and accessibility of biopharmaceutical supply chains.

📋 Description

• Coordinate operations for Resilience-sponsored and investigator-initiated studies across several therapeutic areas • Coordinate day-to-day study operations and logistics • Support planning and follow-up of site selection, initiation, monitoring and close-out visits • Track site progress, study indicators and data quality • Share issues requiring attention during study meetings and governance committees • Follow up on site agreements, amendments and budget annexes • Contribute to site budget tracking and payment follow-up with Legal and Finance • Maintain regulatory documentation and the eTMF • Support audit readiness and ensure compliance with GCP, applicable ICH guidelines, the French Jardé Law and GDPR • Collaborate with Clinical Scientists, Biostatistics, Product, Legal and Finance teams • Improve clinical operations trackers, standard operating procedures and templates • Report to the Clinical Operations Lead

🎯 Requirements

• Degree in life sciences, pharmacy, clinical research or biomedical engineering • At least two years of experience in clinical research, for example as a CRA, site manager or junior project manager • Experience contributing to the operational follow-up of clinical sites or studies • Ability to organize clinical study activities and track priorities, deadlines and actions across stakeholders • Knowledge of GCP, relevant ICH guidelines, the French Jardé Law and GDPR • Ability to maintain structured study documentation and use study indicators to monitor progress • Experience or ability to contribute to regulatory submission follow-up, site contracting and budget tracking • Professional fluency in French and English, written and spoken • Structured, detail-oriented and able to work independently • Ability to prioritize effectively and communicate across functions • Collaborative, adaptable, curious and resourceful approach

🏖️ Benefits

• Fully remote within France • Regular travel related to the role • Opportunity to contribute to studies combining clinical research, digital tools and patient-centered monitoring • Opportunity to develop regulatory and contractual coordination skills • Work across several therapeutic areas with complementary disciplines • Opportunity to improve clinical operations methods and tools • Team celebrations and practical, collaborative problem-solving culture