Clinical Feasibility Leader

🔥 27 minutes ago

🌐 United Kingdom, Hungary, +11 more countries – Remote

🇬🇧 United Kingdom – Remote 🇭🇺 Hungary – Remote 🇬🇪 Georgia – Remote 🇳🇱 Netherlands – Remote 🇨🇭 Switzerland – Remote 🇩🇰 Denmark – Remote 🇫🇮 Finland – Remote 🇸🇪 Sweden – Remote 🇪🇸 Spain – Remote 🇹🇷 Turkey – Remote 🇧🇪 Belgium – Remote 🇷🇸 Serbia – Remote 🇮🇪 Ireland – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🇬🇧 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

• Act as the functional lead responsible for site identification activities across all study types and phases • Develop and implement protocol-specific site identification strategies • Design protocol-specific site questionnaires and analyze investigator responses • Lead locally assigned teams to deliver prequalified sites, including training, survey launch, and issue escalation • Deliver revised enrollment scenarios and final lists of prequalified sites • Prepare slide decks and integrated reports presenting site selection outcomes, methodology, results, and recommendations • Revise protocol feasibility assessments and country selection analyses using post-award data • Manage country clinical operations surveys and compile data into country selection analyses, scenario modeling, and site identification strategies • Contribute to optimized operational strategies for patient recruitment and enrollment scenarios • Present and defend country/site selection strategies and enrollment models in internal and Sponsor meetings • Act as Project Leader on stand-alone feasibility studies under management supervision, including Sponsor liaison, project initiation, resource planning, implementation, milestone tracking, progress reporting, and communication management • Attend Bid Defense and Sponsor Kick-Off Meetings and present feasibility/prequalification services • Serve as Subject Matter Expert for an identified feasibility system, tool, or process

🎯 Requirements

• Relevant clinical research experience in management of international clinical trials, feasibility, and recruitment • Demonstrated clear understanding of country and site feasibility requirements • Previous exposure to development of clinical trial strategy, modeling of enrollment scenarios, and selection of countries/sites • Strong strategic thinking and analytical skills applied to business needs • Excellent interpersonal, verbal, and written communication • Demonstrated leadership and ability to influence others • Problem-solving skills allowing client-focused approach to work • Flexible attitude with respect to work assignments and new learning • Ability to prioritize workload with attention to detail • Willingness to work in a matrix environment and value teamwork • Ability to work independently and in a decentralized reporting model • Fluent in written and spoken English

🏖️ Benefits

• Home based work from select EMEA locations

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