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
ORJuris Doctorate or equivalent with 2+ years of experience in clinical development operations or clinical trial outsourcing
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What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
