Global Study Manager – Oncology

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

🇬🇧 UK Skilled Worker Visa Sponsor

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Logo of Parexel

Parexel

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Manage global study activities from start-up through conduct and study close • Manage study management aspects of assigned studies, including vendor and budget management • Support clinical research activities advancing new patient treatments • Collaborate with global cross-functional teams • Support set-up, execution, and delivery of assigned trials • Contribute to sponsors’ pipeline through accurate planning and efficient trial execution • Implement global study-level start-up and site activation plans • Manage global/regional study-level recruitment strategy • Support development of global study-level plans • Communicate with global and local teams, internal stakeholders, and CRO partners to ensure timely study delivery • Manage and oversee study vendors, including follow-up and coordination of vendor deliverables

🎯 Requirements

• Experienced Global Study Manager with strong oncology trials experience • Extensive experience in clinical trial project management across international trials • Global experience working in clinical research, healthcare, or a regulated environment • Ability to collaborate across teams and communicate clearly • Patient-focused mindset and strong attention to detail • Ability to work independently and exercise own judgement • M.S./M.A./Ph.D. or B.A./B.S./nursing degree is essential (Master’s preferred) • Minimum of 5 years’ relevant experience in clinical trial management • Excellent leadership, communication, and organizational skills • Ability to multitask under limited direction and on own initiative • Strong communication, organization, and problem-solving skills • Fluency in English, both written and spoken • Prior and demonstrable experience working at a senior level within Study start-up is preferred

🏖️ Benefits

• Fully remote home-based position • Flexibility • Growth opportunities • Continuous learning opportunities • Career paths and skills expansion

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