Clinical Project Leader – Senior Project Leader, Mid/Large BioPharma

🔥 0 minutes ago

🇬🇧 United Kingdom – 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

• Lead project delivery for Mid & Large BioPharma clients and their projects globally • Lead Parexel and client teams using clinical research experience and insight into client pressures • Provide overall cross-functional leadership of clinical trials, studies, and project teams • Deliver projects on time, to budget, with high quality and in compliance with ICH GCP • Develop and maintain formal project plans covering milestones, budgets, resources, tasks, and outcomes • Identify project risks, implement contingency plans, mitigate risks, and communicate with clients • Establish project quality standards and drive team commitment to quality • Own study-level client relationships and manage client communications • Manage project P&L, budgets, revenue recognition, forecasting, resources, pass-through costs, scope changes, and invoicing • Manage cross-functional project teams to achieve successful study completion and client satisfaction • Represent Project Leadership in client meetings and presentations, including bid pursuit and investigator meetings • Contribute to SOP reviews and other organizational initiatives

🎯 Requirements

• Bachelor’s degree or equivalent level of education (Science or Medical related field preferred) or proven substantial clinical project management experience • Advanced degree desirable • Strong previous CRO experience • Understanding of Phase I, II-III clinical trial project management • Demonstrable project leadership skills • In-depth knowledge of Oncology; Ophthalmology, Neurology, Dermatology, or NASH desirable • Strong command of written and spoken English language • Strong financial management and client relationship skills • Involvement with bid defense activities • Applications from candidates with pharma experience may also be considered • Familiarity with standard business and eClinical systems used in Clinical Research desirable • Knowledge of ICH and GCP regulations in relevant geographies • Solid clinical knowledge and understanding of clinical research and protocol design • Ability to use Microsoft Excel, PowerPoint, Word, and project planning software • Ability to work in a matrix environment and independently with oversight guidance • Ability to manage multiple tasks, prioritize workload, and maintain high attention to detail • Ability to take a proactive, solutions-based approach • Critical thinking and problem-solving skills • Excellent interpersonal, verbal, and written communication skills • Strong client focus and accountability • Flexible attitude toward assignments and learning

🏖️ Benefits

• Competitive salary • Bonus • Car allowance (country specific) • Benefits package including holiday, pension and other leading-edge benefits • Structured career pathway and development within the role • Awareness and understanding of the industry