In-House Clinical Research Associate

🔥 2 minutes ago

🌐 Poland, United Kingdom, +4 more countries – Remote

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

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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 the Project Manager, traveling CRAs, and Lead CRA on clinical trials • Ensure monitoring activities are properly supported • Track, collect, and review critical documents • Collect, track, and review investigational site records related to subject screening and enrollment • Assist in developing study plans and status reports • Collect, track, and review site regulatory documents • Assist with developing and reviewing Informed Consent Forms • Interact with sites, clients, vendors, and internal study team members • Maintain the CTMS and other project tracking tools • Track study supplies and coordinate shipments to sites as needed • Manage the study Trial Master File and ensure periodic TMF audits • Coordinate work with CRAs conducting on-site monitoring • Perform on-site co-monitoring and remote monitoring activities • Review data entered by investigational site staff according to data review and monitoring guidelines • Assist CRAs with query resolution and data reviews • Ensure studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and federal regulations • Potentially mentor other team members

🎯 Requirements

• Bachelor's degree in a life science, nursing, or pharmacy field • At least 1 year of direct work experience managing essential documents within the CRO, pharma, or biotech industry • Good knowledge of the clinical research process • Understanding of regulatory and central/local ethics submission processes for assigned countries • Working knowledge of current ICH GCP guidelines and applicable regulations • Desire or career goal of growing into a traveling CRA role • Strong written, verbal, and presentation skills • Fluency in both the local language and English • Attention to detail and commitment to high-quality scientific standards • Ability to work collaboratively with honesty and integrity • Critical thinking and objective evaluation skills • Ability to adapt quickly to changing environments • Resume/CV must be submitted in English

🏖️ Benefits

• Work-life balance flexibility • Supportive, collaborative work environment • Financial, workforce, and corporate stability • Career growth and development opportunities • Opportunity to gain experience toward a traveling CRA role • Potential mentoring opportunities

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