Investigator Contracts Lead I – SSU

🔥 1 minute ago

🇹🇼 Taiwan – Remote

⏰ Full Time

🟠 Senior

✨ Investigator

👻 Ghost score 10%

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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

• Exercise good judgment in balancing client risks in budget and contractual decisions against impacts on clinical trial timelines • Develop, negotiate, track, and execute global clinical study agreements with institutions and investigators in sponsored clinical trials • Work with partners to develop and oversee the global site budget process • Negotiate cost, business, and contractual terms with clinical trial sites and investigators/institutions • Lead study-level site contracting activities and act as primary study point of contact for site contracting issues and timelines • Direct other Investigator Contracts Leads • Partner with Legal and other divisions to manage escalations and improve site budgeting and contracting processes • Lead relationships with investigational sites and Site Management Organizations • Collaborate with invoicing specialists or invoice service providers on site contracting and compensation requirements • Interact with clinical site contracts and legal contacts, client and partner legal teams, study management, site payments teams, peer site contracting colleagues, and CRO site contracting teams • Contribute to major business initiatives and special projects • Complete required training, timesheets, expense reports, and CV updates • Maintain knowledge of and comply with Parexel processes, ICH-GCPs, and applicable requirements

🎯 Requirements

• Bachelor’s Degree or equivalent and 5+ years of experience in clinical development operations or clinical trial outsourcing OR Juris Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing • 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 contracting timelines • Ability to lead by influence rather than positional power • Success in working in a highly matrix based organization • Fluency in written and spoken English is required • Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities • Knowledge of principles, concepts and theories in applicable business discipline • Experience drafting and negotiating Clinical Trial Agreements with clinical trial sites in a global operation preferred

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