Fortrea
10,000+ employees
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
Clinical Research Associate II, Phase I
Job not on LinkedIn
đź•’ June 3
🌪️ Kansas, Texas – Remote
đź’µ $105k - $118k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
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Fortrea
10,000+ employees
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
đź“‹ Description
• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites • Conduct pre-study and initiation visits • Ensure informed consent procedures and protocol requirements are adhered to • Monitor data for missing or implausible data • Complete Serious Adverse Event (SAE) reporting • Assist with training of new employees
🎯 Requirements
• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) • 1+ years of Clinical Monitoring experience • Phase I experience • 40-50% overnight travel
🏖️ Benefits
• Health insurance • Flexible work arrangements • Professional development opportunities
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