Senior Clinical Research Associate II – Ophthalmology

🔥 17 minutes ago

🦌 Connecticut, Florida, +8 more states – Remote

🦌 Connecticut – Remote 🐊 Florida – Remote 🗻 New Hampshire – Remote 🏖️ New Jersey – Remote 🗽 New York – Remote 🏈 Ohio – Remote 🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote 🎸 Tennessee – Remote ⚔️ Virginia – Remote

💵 $125k - $142k / 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

• Provide a high standard of care for participants in clinical trials and respond to emergency situations based on clinical research standards • Conduct all aspects of study site monitoring, including routine monitoring and close-out of clinical sites • Maintain study files and 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 regulations • Ensure integrity of data submitted on Case Report Forms and other data collection tools • Monitor data for missing or implausible data • Manage registries and undertake feasibility work when requested • Complete Serious Adverse Event reporting, reports, narratives, and follow-up • Perform CRF review and query generation and resolution in Fortrea or client data management systems • Assist with training new employees through co-monitoring • Coordinate designated clinical projects as a Local Project Coordinator • Act as a local client contact when assigned • Perform other duties assigned by management

🎯 Requirements

• Residing on the East Coast of the US • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) • 5+ years of Clinical Monitoring experience • Oncology experience preferred, especially early phase • 30-50% overnight travel • Ability to work in a fast-paced, changing-priority, 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, stooping, 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, luggage, and laptop computer, up to 15-20 lbs • Regular and consistent attendance • Varied hours may be required

🏖️ Benefits

• Remote work arrangement • Ongoing application acceptance