Senior Clinical Research Associate II – Oncology

🕒 August 10

⛰️ Colorado – Remote

⛰️ Colorado – Remote

💵 $125k - $140k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 13%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 • Perform 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 and manage study sites according to project plans • Ensure study staff receive proper materials and instructions for safely entering patients into studies • Verify informed consent procedures and protocol requirements comply with applicable regulations • Ensure integrity of CRF and other collected data through source-document review • Monitor data for missing or implausible values • Manage registries according to project plans • Undertake feasibility work when requested • Complete SAE reporting, reports, narratives, and follow-up • Perform CRF review, 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

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution • Example qualifying credential: nursing licensure • 5+ years of clinical monitoring experience • Oncology experience; early phase preferred • Ability to travel overnight 30–50% of the time • Comfortable working in a fast-paced, constantly changing, technology-based environment • Ability to work with electronic data-collection environments • Ability to sit for extended periods and operate a vehicle safely • Ability to perform repetitive hand movements and fast, simple, repeated finger, hand, and wrist movements • Ability to crouch, stoop, bend, and twist the upper body and neck • Ability to use in-house and off-the-shelf computer software • Ability to lift and carry luggage and a laptop weighing up to 15–20 lbs • Regular and consistent attendance • Varied hours may be required

🏖️ Benefits

• Target pay range of $125 - $140K • Remote work arrangement • Ongoing application acceptance • EEO and accommodations support • Global Talent Network opportunity