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Parexel

End-to-end clinical trials and regulatory consulting

Site Payment Lead

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in ArgentinaNo salary listedRemote

About the Job

Requirements

  • A minimum bachelor's degree or equivalent degree is required.
  • Non-native English speakers must have an advanced to excellent level of English.
  • At least 4 years of experience are preferred in a Clinical Research Organization, business, finance/accounting, or comparable work.
  • Experience supporting Clinical Site Payments is required.
  • Strong interpersonal, verbal, and written communication skills are required.
  • Ability to make decisions and advise staff in ambiguous situations is required.
  • Ability to conduct root cause analysis for problem solving and process development is required.
  • Strong customer focus and professional interaction are required.
  • Ability to manage multiple varied tasks, prioritize workload, and attend to detail is required.
  • Expert-level proficiency in Microsoft Excel for spreadsheet analysis is required.
  • Strong proficiency in Microsoft Outlook, Teams, PowerPoint, and Word is required.
  • A analytical mindset and attention to detail are required.
  • Commitment to high-quality work and consistent performance is required.
  • Ability to work in a decentralized matrix environment and collaborate as a team member is required.
  • Understanding of typical work deliverables and the fundamentals of the CRO industry, including how Investigator Payments influence the organization, is required.
  • Thorough knowledge of the company's standard operating procedures, operational guidelines, and work instructions is required.
  • In-depth understanding of payment setup and payment processes, including the ability to analyze agreements, is required.
  • Knowledge of clinical trial pricing and budgeting tools and how operational changes are reflected in those tools is required.

Responsibilities

  • Serve as the accountable lead and point of contact for Site Payment Services queries on assigned studies.
  • Solve customer problems proactively and accept responsibility for actions.
  • Work with Project Leadership, Global Site Contracts, eClinical Business Implementation, Global Clinical Operations, and Site Payment Services colleagues to obtain information needed to perform tasks.
  • Represent the Investigator Payment team in study start-up and payment strategy meetings, ensuring initial funding setup requirements are documented for payment processing.
  • Lead and follow up on audits and inspections.
  • Complete administrative tasks, including timesheets, metrics, and expenses, in a timely manner.
  • Collect needed information from teams, systems, and tools proactively and on time.
  • Analyze and present data to stakeholders.
  • Train Site Payment Services team members.
  • Identify and implement process efficiencies.
  • Manage end-to-end site payments and keep internal and external team members informed about payment status and issues.
  • Authorize study setups accurately before payments begin.
  • Resolve escalated second-line helpdesk issues for the assigned portfolio.
  • Assist in preparing project status reports as needed.
  • Work with IFA and the project team to ensure appropriate funding before administering payments.
  • Participate proactively in Project Strategy Meetings and contribute to payment strategy planning for incoming studies.
  • Meet investigator payment timelines specified in contractual terms.
  • Resolve payment discrepancies to ensure accurate processing.
  • Provide payment reports for assigned projects to customers upon request.

Desired Qualifications

  • At least 4 years of experience in a Clinical Research Organization, business, finance/accounting, or comparable work is preferred.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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