Senior CRA, Oncology, Multi-Specialty TAs

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🔥 5 minutes ago

🌐 United States, Philippines – Remote

🇺🇸 United States – Remote 🇵🇭 Philippines – Remote

🏄 California, Connecticut, +19 more states – Remote

🏄 California – Remote 🦌 Connecticut – Remote 🐊 Florida – Remote 🌽 Illinois – Remote 🏖️ New Jersey – Remote 🗽 New York – Remote 🌾 North Dakota – Remote 🏈 Ohio – Remote 🌪️ Oklahoma – Remote 🦀 Maryland – Remote 🍂 Massachusetts – Remote 🚗 Michigan – Remote ❄️ Minnesota – Remote 🏰 Missouri – Remote 🗿 South Dakota – Remote 🎸 Tennessee – Remote 🤠 Texas – Remote ⚔️ Virginia – Remote ☕ Washington – Remote 🧀 Wisconsin – Remote 🍑 Georgia – Remote

💵 $110k - $118k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 0%

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Conduct routine monitoring and close-out of clinical sites • Maintain study files • Conduct pre-study and initiation visits • Liaise with vendors • Manage study sites according to project plans • Ensure study staff receive proper materials and instructions • Verify informed consent procedures and protocol requirements comply with applicable regulations • Verify integrity of data submitted on CRFs and other data collection tools • Monitor data for missing or implausible data • Manage registries and undertake feasibility work when requested • Complete SAE reporting, reports, narratives, and follow-up • Perform CRF review and generate and resolve queries in Fortrea or client data management systems • Assist with training new employees through co-monitoring • Coordinate designated clinical projects as a Local Project Coordinator, with supervision if applicable • Act as a local client contact as assigned • Travel frequently to client and site locations, including occasional domestic and international travel • Perform other duties as assigned by management

🎯 Requirements

• 2+ years of monitoring experience • 3+ years of Clinical Monitoring experience • Oncology monitoring experience desired • Ophthalmology experience • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) • 30-50+% overnight travel • Ability to work in a fast-paced, constantly changing, technology-based environment • Teamwork and people skills • Ability to sit for extended periods and operate a vehicle safely • Repetitive hand movement of both hands and ability to make fast, simple, repeated movements of the fingers, hands, and wrists • Occasional crouching and stooping, with frequent bending and twisting of upper body and neck • Ability to access and use a variety of computer software • Light to moderate lifting and carrying of objects including luggage and laptop computer, up to 15-20 lbs • Regular and consistent attendance • Varied hours may be required

🏖️ Benefits

• Regionalized travel as possible • No hard metrics • Ongoing application acceptance • EEO and accommodations support

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