Clinical Research Associate

🔥 16 hours ago

🇺🇸 United States – Remote

💵 $55k - $65k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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

• Collect, track and review investigational site records relating to subject screening and enrollment • Assist in the development of study plans and status reports • Collect, track, and review all site regulatory documents • Assist with development and review of Informed Consent Forms • Interact with sites, clients, vendors and internal study team members • Maintain the clinical trials management system (CTMS) and other project tracking tools • Track study supplies and coordinate shipments of supplies to sites as needed • Manage the study Trial Master File (TMF) and ensure periodic TMF audits • Coordinate work with CRAs monitoring on-site • Perform on site co-monitoring and remote monitoring activities • Perform regular reviews of data entered by investigational site staff according to data review/monitoring guidelines • Work with the Project Manager, traveling CRAs and Lead CRA to support clinical trial monitoring activities • 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

• Bachelors 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 clinical research process • Understanding of Regulatory and Central/Local ethic submission processes for assigned countries • Working knowledge of current ICH GCP guidelines and applicable regulations • Desire / Career Goal of growing into a traveling CRA role • Strong written, verbal and presentation skills • Attention to detail and understanding of high-quality scientific standards • Honesty and integrity • Ability to evaluate situations objectively and incisively and craft novel, practical solutions • Ability to change quickly and adapt to evolving environments

🏖️ Benefits

• Medical insurance • Vision insurance • Dental insurance • HSA • FSA • EAP • Life insurance • Disability insurance • 401(k) • Paid time off • Holidays • Parental leave • Bereavement leave • Work-life balance flexibility

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