FSP CRA 2 – Senior CRA, Oncology

🔥 1 hour ago

🏄 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

💵 $118k - $145k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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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

• Provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards • Perform all aspects of study site monitoring, including 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 to safely enroll patients • Verify informed consent procedures and protocol requirements comply with applicable regulatory requirements • Ensure integrity of data submitted on Case Report Forms and other data collection tools • Monitor data for missing or implausible information • Manage registries according to project plans and undertake feasibility work when requested • Complete Serious Adverse Event reporting, including reports, narratives, and follow-up • Independently perform CRF review, query generation, and query resolution using 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 • Perform other duties as assigned by management • Travel frequently to client and site locations, including occasional domestic and international travel

🎯 Requirements

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) • 3+ years of Clinical Monitoring experience • Oncology expertise required • Ophthalmology experience • Ability to travel overnight 30-50+% of the time • Comfortable working in a fast-paced, protocol-driven environment • Ability to adapt to changing priorities • Teamwork and people skills • Ability to work in a technology-based electronic data environment • Ability to sit for extended periods and operate a vehicle safely • Ability to perform repetitive hand movements • Ability to crouch, stoop, bend, and twist • Ability to use in-house and off-the-shelf computer software • Ability to lift and carry 15-20 lbs. • Regular and consistent attendance • Varied hours may be required

🏖️ Benefits

• Remote work arrangement • 30-50+% overnight travel • Occasional domestic and international travel

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