Associate Clinical Team Lead

🔥 7 hours ago

🌐 Spain, Poland, +2 more countries – Remote

🇪🇸 Spain – Remote 🇵🇱 Poland – Remote 🇬🇧 United Kingdom – Remote 🇱🇻 Latvia – Remote

⏰ Full Time

🟠 Senior

✨ Team Lead

👻 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

• Support CTLs in end-to-end clinical execution of projects or programs, ensuring adherence to protocols, timelines, and regulatory requirements • Track and monitor recruitment, study metrics, monitoring, and documentation activities • Apply ICH-GCP and ensure sites comply with GCP and applicable regulations • Collaborate with data management, regulatory, safety, and other cross-functional teams • Support clinical operation timelines, metrics, resourcing, budgets, and activities • Identify risks and implement corrective actions and mitigation strategies • Track and reconcile clinical operation budgets, including monitoring visits and CRA allocation • Support communication among clients, site staff, and internal teams; escalate issues to CTL and study teams • Assist with internal and external meetings and routine client communications • Assist with CRA and IHCRA training, onboarding, and preparation of training materials • Foster collaboration and integration across project teams and sites • Provide performance feedback on CRAs/IHCRAs to line managers and project leads • Support protocol deviation review and reconciliation activities • Assist with project-specific training compliance and study protocol/document development • Support planning and execution of on-site Quality Compliance Visits under study team guidance • Keep up with industry trends, regulatory changes, and standard practices

🎯 Requirements

• Bachelor's Degree, preferably in a life science, nursing, pharmacy or related field • 3 years of clinical research experience within the CRO, pharmaceutical, or biotechnology industry • At least 2 years of on-site monitoring experience • Proven leadership capabilities with experience leading teams within a CRO or pharmaceutical setting • Strong knowledge of GCP and regulatory requirements • Familiarity with clinical trial processes and documentation • Excellent interpersonal and communication skills • Ability to manage multiple priorities and deliver on deadlines in a fast-paced environment • Proactive, solutions-oriented mindset with ability to drive decisions and lead initiatives • Experience using clinical trial management software and EDC systems • CV must be submitted in English

🏖️ Benefits

• Work-life balance flexibility • Supportive, collaborative work environment • Stability and long-term career development opportunities • Remote work arrangement • Occasional travel for site visits and client meetings