Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Investigator Contracts Lead I- FSP (Dedicated to client office)
Job ID R0000034963 , TaiwanKey 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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