Clinical Project Leader – Senior Project Leader, Biotech

🔥 7 minutes ago

🌐 United Kingdom, Ireland, +6 more countries – Remote

🇬🇧 United Kingdom – Remote 🇮🇪 Ireland – Remote 🇵🇱 Poland – Remote 🇷🇴 Romania – Remote 🇪🇸 Spain – Remote 🇭🇺 Hungary – Remote 🇭🇷 Croatia – Remote 🇱🇹 Lithuania – Remote

⏰ Full Time

🟠 Senior

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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

• Independently responsible for all Project Leader tasks and deliverables according to SOPs on assigned projects • Develop and maintain a formal project plan with all key milestones, budgets, and resources assigned to specific tasks and outcomes • Perform initial and ongoing risk management: Identify potential project risks and implement contingency plans, mitigate actual risks with team members and keep client informed about risks and contingencies • Manage and ensure first time quality on the project deliverables: Establish quality standards for the project that drive individual and team commitment to quality • Develop and manage the client relationship: Owns the client relationship at a study level and responsible for client communication ensuring high client satisfaction • Understand and own the project P&L: Manage the project according to budget with revenue recognition and forecasting, including resource management, pass-through management (review, regular reconciliation and forecasting) as well as managing Change in Scope and all project invoicing activities • Manage the cross-functional project team: Enable all stakeholders to achieve successful study completion while maintaining high client satisfaction • Represent Project Leadership function in external client meetings and presentations such as Bid Pursuit Meetings, Investigator Meetings or others as required

🎯 Requirements

• Bachelor’s degree or equivalent level of education (Science or Medical related field preferred) • Advanced degree desirable • Ability to take a proactive, solutions-based approach • Critical thinking & problem-solving • Excellent interpersonal, verbal and written communication skills • Highly accountable with a strong client focus • A flexible attitude with respect to assignments and new learning • Ability to manage multiple and varied tasks with enthusiasm and be able to prioritize workload with high attention to detail • Ability to work in a matrix environment and to value the importance of teamwork and collaboration • Basic understanding of all aspects of the project life cycle • Ability to work independently with oversight guidance • Proficient in Microsoft Excel, Power Point, and Word, and project planning software • Strong previous CRO experience and understanding of Phase I, II-III clinical trial project management with demonstrable project leadership skills are essential • In-depth knowledge of the Therapeutic Areas: Oncology is essential plus any of the following Dermatology, Women's Health, Neurology, Rare Disease, Radiopharmaceuticals are desirable • Strong command of written and spoken English language is essential • Strong financial management and client relationship skills as well as involvement with bid defense activities are essential • Familiarity with standard business and eClinical systems used in Clinical Research is desirable • ICH and GCP regulations in relevant geographies • Solid clinical knowledge and understanding of clinical research and protocol design.

🏖️ Benefits

• Competitive salary • Bonus • Car allowance (country specific) • Holiday • Pension • Leading-edge benefits