Clinical Project Leader – Biotech

🔥 4 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Healthcare Insurance • Biotechnology • Pharmaceuticals

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

• Lead project delivery and oversight for Biotech clients globally. • Develop and maintain formal project plans with milestones, budgets, and resources. • Identify project risks and implement contingency plans. • Establish quality standards and drive commitment to project deliverables. • Own the client relationship and ensure high satisfaction. • Manage project P&L, revenue recognition, and budgeting. • Enable all stakeholders for successful study completion. • Represent Project Leadership function in client meetings and presentations.

🎯 Requirements

• Therapeutic Area expertise in Oncology and any of the following: Dermatology, Women's Health, Neurology, Rare Disease or Radiopharmaceuticals. • Bachelor’s degree or equivalent in Science or Medical related field preferred, or proven substantial clinical project management experience. • Advanced degree desirable. • Ability to take a proactive, solutions-based approach. • Critical thinking & problem-solving skills. • Excellent interpersonal, verbal and written communication skills. • Strong client focus. • Flexibility in assignments and learning. • Ability to manage multiple tasks with detail orientation. • Ability to work independently with oversight guidance. • Proficient in Microsoft Excel, Power Point, Word, and project planning software. • Strong previous CRO experience with Phase I, II-III clinical trial project management.

🏖️ Benefits

• Competitive salary • Bonus • Car allowance is country specific • Holiday • Pension • Other leading-edge benefits