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Location
Remote (Argentina)
Seniority
Staff · 4+ years exp

Confirmed on the employer's own hiring board on Oct 20, 2026. First seen by Alion on Sep 9, 2026. Parexel scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Parexel is a clinical research organisation headquartered in Durham, North Carolina that provides Phase I to IV clinical trial services, regulatory consulting, market access and safety services to biopharmaceutical companies. Founded in 1983 and owned by EQT and Goldman Sachs since 2021, it employs more than 21,000 people, with large teams in the US, Hyderabad, Bengaluru, London, Poland, Romania, Serbia and Bloemfontein. Its openings are mostly for regulatory affairs consultants and associates, clinical research associates, safety technology analysts, clinical trial managers, data and AI engineers, many of them home or office based.

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.

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose - moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.

About the Role

We are seeking a Site Payment Lead to join our team in a remotecapacityThe Site Payment Lead is responsible for coordinating with the team members and their activities across studies, liaising with the project teams to ensure set-up and site payments are effectively managed; and is accountable for the management of payments for the assigned studies. This includes the accountability for payment setup and modifications within the investigator payment system for expenses aligned to budget templates.

Working independently, they will show an elevated level of ownership assisting the project team project planning, decision making process and timely payments to investigator sites. As a dedicated team player, the Site Payment Lead provides excellent proactive support across projects and tasks as assigned with supervision, identifying risks, their impact, and potential resolutions.

Key Accountabilities:

Overall Accountabilities:

  • Be the accountable Lead for Site Payment Services related queries on assigned studies and point of contact for project teams.

  • Proactively and effectively solves customer problems and accepts responsibility for actions.

  • Work closely with Project Leadership, Global Site Contracts, eClinical Business Implementation, Global Clinical Operations, and other internal Site Payment Services team members to obtain additional information required to perform tasks, when applicable.

  • Participate as the Lead representative of the Investigator Payment team in study start-up meetings, including payment strategy meetings, to ensure initial funds setup requirements are documented for seamless payment processing.

  • Lead and follow-up on audits/inspections

  • Knowledge of clinical trial pricing/budgeting tools and how to reflect operational changes within the tools

  • Thorough knowledge of Parexel’s SOPs, Operational Guidelines and Work Instructions procedures.

  • Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, and expenses).

  • In depth understanding of the set-up and payment process; including ability to analyze agreements.

  • Collection of information from all teams/systems/tools wherever needed on a timely and proactive basis.

  • Analyze and present data to various stakeholders.

  • Trains team members within the Site Payment Services.

  • Discover and implement opportunities for process efficiencies.

End to end management of Site Payments:

  • Keeps internal and external team members aware of site payment status and issues.

  • Accurately authorize study setups before starting payments.

  • Resolve escalated second line helpdesk issues for assigned portfolio.

  • Assist in the preparation of project status reports as needed.

  • Works with IFA and project team to ensure appropriate funding prior to administering payments.

  • Proactively participates in Project Strategy Meetings (PSM), providing input to payment strategy planning for incoming studies.

  • Compliance with the Investigator payment timelines as per the contractual terms.

  • Resolve payment discrepancies to ensure accurate processing of payments.

  • Provide payments reports for assigned projects to customers as requested.

Skills:

  • Strong interpersonal, verbal, and written communication skills.

  • Ability to make decisions and advise other staff even in ambiguous situations.

  • Ability to conduct root cause analysis in problem solving and process development.

  • Strong customer focus, ability to interact professionally.

  • Patient, Quality and Client focused approach to work.

  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.

  • Expert in using MS Excel for spreadsheet analysis.

  • Strong proficiency in use of MS Outlook, Teams, PowerPoint, and Word.

  • Analytical mind with strong attention to detail.

  • Commitment to high quality work and consistent performance.

  • Comfortable with working in a decentralized matrix environment and being a conversant team player.

  • Delivers standard/typical work deliverables without issues.

  • Thoroughly understands fundamentals of CRO industry and how Investigator Payments influence in the organization.

Knowledge and Experience:

  • 4+ years’ experience are preferred within a Clinical Research Organization; Business; Finance/Accounting; or other comparable experience.

  • Must have experience supporting Clinical Site Payments

Education:

  • Advanced to excellent English level for non-native English speakers.

  • Minimum bachelor’s degree or equivalent degree.

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

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