Global Project Manager – Respiratory

🔥 4 minutes ago

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

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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

• Lead global Phase II and III respiratory clinical studies within a CRO or sponsor environment • Manage complex, multi-country clinical trials, overseeing timelines, budgets, risks, resources, and sponsor relationships • Serve as a primary client contact • Lead cross-functional global teams • Operationally oversee complex respiratory endpoint vendors • Apply ICH-GCP, clinical operations, study start-up, enrollment management, and vendor oversight practices • Contribute to bid defense, proposal strategy, and client governance • Lead or mentor PMs and junior team members • Support decentralized, digital, or innovative trial delivery models • Drive strategic problem-solving and proactive risk management • Lead through complexity and change • Support respiratory portfolios for major pharma sponsors • Manage global studies involving hundreds of sites and multiple regions • Conduct study rescue, accelerated start-up, or enrollment recovery programs • Coordinate clinical operations, medical, regulatory, and vendor partners

🎯 Requirements

• Experienced EU-based Respiratory Project Manager or Senior Project Manager experience • Strong respiratory therapeutic expertise, ideally including asthma, COPD, ILD, severe respiratory disease, pulmonary fibrosis, or related indications • Experience leading global Phase II and III studies within a CRO or sponsor environment • Ability to manage complex, multi-country clinical trials, including timelines, budgets, risks, resources, and sponsor relationships • Strong understanding of ICH-GCP, clinical operations, study start-up, enrollment management, and vendor oversight • Experience serving as a primary client contact and leading cross-functional global teams • Ability to operate independently and manage complex stakeholder environments • Experience operationally overseeing complex respiratory endpoint vendors • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution • Relevant and equivalent experience may be considered in lieu of educational requirements • Preferred: overall respiratory expertise including rare respiratory (IPF) and specialized respiratory populations • Preferred: large global programs with accelerated timelines and high enrollment demands • Preferred: RBQM and risk-based delivery approaches • Preferred: bid defense, proposal strategy, and client governance experience • Preferred: previous leadership or mentoring responsibilities for PMs and junior team members • Preferred: exposure to decentralized, digital, or innovative trial delivery models • Strong sponsor-facing presence • Strategic problem-solving and proactive risk management • Ability to lead through complexity and change • Commercial awareness and growth mindset • Collaborative leadership style • Experience with respiratory portfolios for major pharma sponsors • Experience with global studies involving hundreds of sites and multiple regions • Experience with study rescue, accelerated start-up, or enrollment recovery programs • Cross-functional leadership across clinical operations, medical, regulatory, and vendor partners • Preferred: Master’s or other advanced degree • Preferred: PMP certification