Investigator Contracts Lead

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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

• Responsible for direct site facing contract and budget negotiations through contract execution with assigned clinical investigator sites • Manage the Per-Subject Cost (PSC) process for assigned studies • Manage escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (pCRO) • Collaborate with other lines to plan site contracting timelines through start-up • Exercise good judgment in balancing the risks to the sponsor in making budget and contractual decisions against the impacts to client clinical trial timelines • Follow processes to develop, negotiate, track, and execute global clinical study agreements • Work with partners to develop and oversee the global site budget process • Lead study level site contracting activities and act as primary study point of contact for site contracting issues

🎯 Requirements

• At least 3 years of experience with clinical study budgets and contracts negotiation • Fluent in Spanish, Italian and English is a must • Experience in drafting and negotiation of Clinical Trial Agreements with clinical trial sites in a global operation is preferred • Balance of general business, compliance, finance, legal, and drug development experience • Precise communications and presentation skills • Ability to plan, identify and mitigate risks to site contacting timelines • Ability to lead by influence rather than positional power to accomplish critical deliverables • Success in working in a highly matrix-based organization • Fluency in written and spoken English is required

🏖️ Benefits

• Medical care plan: Health, Dental & Vision • Life Assurance • Excellent work environment • Culture of teamwork and collaboration • People who motivate and face challenges together • Innovative technology • Excellent training