Fortrea
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.
Project Manager II
Job not on LinkedIn
🕒 May 14
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Fortrea
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.
📋 Description
• Lead the end-to-end delivery of assigned Healthy Volunteers and Patient Clinical Pharmacology projects • Act as the primary point of contact for sponsor project teams • Own project scope, timelines, and budgets • Anticipate, identify, and mitigate risks to ensure milestones are met • Provide senior leadership guiding and mentoring project team members • Ensure quality, compliance, and audit readiness
🎯 Requirements
• Extensive clinical research experience within a CRO or biopharmaceutical environment • At least 2 years of full project management accountability on clinical studies • Familiarity with early-phase trials in healthy volunteers and patients • Study budget management skills • Proven ability to manage globally dispersed teams • Expertise in critical path analysis and risk mitigation plans • University/college life science degree from accredited institution • Preferred: Master´s or other advanced degree • PMP certification
🏖️ Benefits
• Flexible working hours • Professional development opportunities
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