Investigator Contracts Lead I- FSP (Dedicated to client office)

Client PartnerSalesFull TimeRemoteLeadTeam 10,001+Since 1983H1B SponsorCompany SiteLinkedIn

Location

Taiwan

Posted

71 days ago

Salary

0

Seniority

Lead

Job Description

Investigator Contracts Lead I- FSP (Dedicated to client office)

Parexel

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: Contracting Deliverables - Exercise sound judgment in balancing client risk with clinical trial timeline impacts when making budget and contractual decisions - Follow client-specific processes to develop, negotiate, track, and execute global clinical study agreements with institutions and investigators - Collaborate with internal and external partners to develop and oversee the global site budget process - Negotiate directly with clinical trial sites on cost, business, and contractual terms, making template adjustments within Legal-approved parameters - Lead study-level site contracting activities, guide other contract leads, and serve as the primary contact for site contracting issues and timelines on assigned studies - Partner with Legal and other departments to manage escalations related to site budgeting and contracting - Work with Legal, Finance, pCRO, and other stakeholders to identify and implement improvements in the site contracting process - Apply acquired job skills and procedures to complete assignments and projects of moderate scope and complexity Collaboration - Build and maintain relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface - Collaborate with invoicing specialists and service providers to ensure alignment with site contracting and compensation requirements - Interface with site legal contacts, client legal teams, study management, site payments teams, peer contracting colleagues, and CRO contracting teams - Contribute to the design, development, and implementation of major business initiatives or special projects, applying technical expertise to support client objectives Skills and Competencies - Strong balance of business, compliance, finance, legal, and drug development knowledge - Clear and precise communication and presentation skills - Ability to plan, identify, and mitigate risks to site contracting timelines - Capable of leading through influence rather than authority to achieve key deliverables - Proven success in a highly matrixed organizational environment - Fluency in written and spoken English is required Knowledge and Experience - Experience with clinical study budgets and contract negotiation principles, practices, and processes - Understanding of core concepts and theories in relevant business disciplines - Preferred experience in drafting and negotiating Clinical Trial Agreements with global clinical trial sites Education - Bachelor’s degree or equivalent with 5+ years of experience in clinical development operations or clinical trial outsourcing OR - Juris Doctorate or equivalent with 2+ years of experience in clinical development operations or clinical trial outsourcing

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