Global Study Manager – 6 Month FTC

🔥 17 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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Parexel

WebsiteLinkedInAll Job Openings

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-level implementation of Start-up and Site Activation Plans • Develop and support 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 efficient and timely study delivery • Manage and oversee study vendors, including follow-up and coordination of vendor deliverables • Support clinical research activities that advance new treatments for patients • Contribute to the set-up, execution, and delivery of assigned trials • Contribute to delivery of the sponsor’s pipeline through accurate planning and efficient trial execution

🎯 Requirements

• 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 • Minimum of 5 years’ relevant experience in clinical trial management • Excellent leadership, communication, and organizational skills • Ability to multi-task 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

• 6-month fixed term contract • Fully remote, home-based position • Flexibility • Growth and continuous learning opportunities • Opportunities to explore career paths and expand skills across clinical research