Investigator Contracts Lead II

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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

• Serve as a site-facing lead for contract and budget negotiations through contract execution with assigned clinical investigator sites • Manage initial agreements, amendments, and oversight of other contracting professionals on assigned studies • Manage the Per-Subject Cost (PSC) process for assigned studies • Escalate and resolve budget and non-legal term issues from ICLs or preferred CROs • Collaborate across functions to plan site contracting timelines through study start-up • Act as a point of contact for high-priority, complex, or unique contracting structures and strategies • Develop, negotiate, track, and execute global clinical study agreements • Develop and oversee the global site budget process with partners • Negotiate cost, business, and contractual terms with investigators and institutions • Lead ICL, pCRO, and FSP negotiators in achieving study goals • Act as primary study point of contact for site contracting issues and timelines • Partner with Legal, Finance, pCRO, and other divisions on escalations and process improvements • Build relationships with investigational sites and Site Management Organizations • Collaborate with invoicing specialists to align site contracting and compensation requirements • Contribute to major business initiatives and special projects

🎯 Requirements

• At least 7 years of experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities • Experience drafting and negotiating Clinical Trial Agreements with clinical trial sites in a global operation preferred • General business, compliance, finance, legal, and drug development experience • Precise communication and presentation skills • Ability to plan, identify, and mitigate risks to site contracting timelines • Ability to lead by influence rather than positional power • Experience working successfully in a highly matrix-based organization • Fluency in written and spoken English required • Bachelor’s Degree or equivalent and 7+ years of experience in clinical development operations or clinical trial outsourcing, OR Master’s Degree or equivalent and 5+ years of experience, OR Juris Doctorate or equivalent and 2+ years of experience

🏖️ Benefits

• 100% remote work • Healthy work-life balance • Local support • Flexible work environment • Industry-leading growth potential • Meaningful work supporting patients and the development of medicines and therapies