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.
Parexel FSP is looking to hire multiple Site Payment Specialists in Argentina and Mexico
Provide broad support of payment and budget configurations and setup of payment systems.
JOB RESPONSIBILITIES
Work with the Sponsor’s Investigator Payments Lead (“IPL”) to ensure the payment requirements are clearly delineated and defined for each study
Review and interpret global clinical payment documents for each contract executed (CSAs, budgets, amendments, and Budget Modification Letters) and extract payment information for budget configuration template (e.g. amounts, caps, limits, backup requirements, etc.)
Endeavor to ensure sites are set up correctly for payment in IPS payment system
Distinguish between data driven and manual payment line items and configure accordingly
Escalate and timely resolution of ambiguous payment information to contract negotiators for clarification
Follow up with sites on relevant payee form completion, correction, or modification
Collaborate and communicate with business partners
Endeavor to ensure adherence to sponsor’s processes
Create and upload completed budget configuration template to IPS Supplier within an average of three (3) business days of receipt of fully executed CSA, Excel budget, and other payment support forms. In the event any issues or delays arise in this process, the parties will work together in good faith to resolve any such issues or delays.
Partner with Investigator Payments Lead (IPL) to track missing and incomplete documents
Track all issues and resolution
Attend payments study team calls as needed
QUALIFICATIONS / SKILLS
BS degree or extended relevant industry experience
2+ years' experience working in a related discipline.
Business or technical degree is preferred along with basic clinical trial knowledge
Written and oral language fluency in legal, medical, and scientific terms
Fluent in English and at least one other European language. Fluency in local language(s)
Strong Excel skills
Previous project management experience is preferred
Strong communication skills
Attention to detail evident in a disciplined approach to contracts, budgets, and management
Understand budget and payment setup configurations
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 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.
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