Senior Analyst, Site Contracts and Budgets

November 8

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Parexel

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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.

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

📋 Description

• Negotiate and maintain Clinical Trials Agreements, site budgets, and other applicable contracts • Oversee CRO or Functional Service Provider in budget development • Ensure compliance with Fair Market Value principles • Track contract progress and coordinate completion of contracts • Collaborate with cross-functional teams in executing contracts • Develop and analyze tools and systems to manage contract lifecycle • Provide guidance to new clinical operations and outsourcing team members • Ensure adherence to department guidelines and templates • Assist management with process improvement projects

🎯 Requirements

• 3 – 5 years’ experience in the pharmaceutical or biotechnology industry in clinical site contracts and/or outsourcing management • Proficient with Excel and PowerPoint • Excellent verbal, written and interpersonal communication skills • Willingness to learn international clinical pharmaceutical standards, ICH/GCP guidelines and regulatory compliance issues • Strong interest in contracts and budgeting in support of Sponsor clinical trials • Working knowledge of clinical trial functions, including clinical operations, regulatory and drug safety • Ability to prioritize and manage multiple tasks simultaneously • Fluent in spoken and written German and English is essential • Advanced spoken and written Polish skills preferred • Turkish, Portuguese or Russian language skills as desirable alternatives to Polish language skills

🏖️ Benefits

• Tremendous long-term job security and prospects • Opportunity to develop within your role and tackle further responsibilities • Development of skills within other related departments