
10,000+ employees
🧬 Biotechnology
💊 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.
🔥 3 hours ago
🇺🇸 United States – Remote
💵 $80k - $89k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
💸 Financial Planning and Analysis (FP&A)
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10,000+ employees
🧬 Biotechnology
💊 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.
• Develop Clinical Trial Agreements (CTAs) utilizing standard templates • Ensure CTAs are executed timely • Liaise with legal departments for content changes • Participate in Study kick-off meetings • Generate site budgets based on final approved country budget • Manage CTAs ensuring changes are updated • Responsible for internal approval forms and compliance • Ensure communication among trial site personnel • Negotiate Master Services Agreements (MSAs) with Institutions • Support Country Study site budget template, parameter, and payment term building
• Must have 2+ years of budget/contract negotiation experience at CRO level • Direct site facing experience • Experience building global budget templates • Must have a Bachelor’s degree or equivalent scientific or commercial Higher Vocational education • Experience in the healthcare field, pharmaceutical industry or clinical research preferred
• Medical, Dental, Vision, Life insurance • STD/LTD • 401(K) • ESPP • Paid time off (PTO) or Flexible time off (FTO) • Company bonus where applicable
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