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Parexel

End-to-end clinical trials and regulatory consulting

Site Payment Associate

Project ManagementConfirmed live in the last 24 hours
Full-timeNo salary listedIn-person

About the Job

Requirements

  • Advanced English proficiency is required for non-native English speakers.
  • A minimum of two years' experience in a PS II role or an equivalent role is required.
  • An in-depth understanding of how the role integrates with other business functions to accomplish project deliverables and area objectives is required.
  • An excellent understanding of project management and applicable tools is required.
  • A developed financial understanding is required.
  • Mentoring or training experience is required.
  • A basic understanding of the business and market is required.
  • ICH/GCP knowledge is required.
  • A minimum Bachelor's degree or equivalent degree is required.
  • Excellent interpersonal, verbal, and written communication skills are required because exchanging information is a significant part of the job.
  • Attention to detail and an understanding of how work quality affects others and business outcomes are required.
  • A client-focused approach to work is required.
  • A flexible attitude toward work assignments is required.
  • Openness to learning and role-modeling adoption of change are required.
  • The ability to manage multiple varied tasks and teach others in these tasks is required.
  • Willingness to work in a matrix environment and value teamwork is required.
  • The ability to facilitate cross-functional teamwork toward a goal is required.
  • Excellent problem-solving skills are required.
  • The ability to apply analytical thinking to resolve issues in complex situations is required.

Responsibilities

  • Set up and maintain Project Management Plans with input from the Project Leader and Functional Leads, communicate the plans to the wider project team, and support their execution.
  • Maintain selected information in the integrated project management system and lead cross-functional work to ensure project-system data compliance.
  • Prepare project reports, compliance and other metrics for operational reviews, client and internal reporting, and project oversight; analyze data and initiate and follow up on required actions with Project Leaders and Functional Leads.
  • Review selected financial areas, follow up with stakeholders on corrections, and provide reconciliations to the Project Leader as agreed.
  • Coordinate with the Project Leader and Functional Leads on action plans and follow up with the project team through completion.
  • Oversee project team lists, system access, and access reviews; develop related processes and roll them out to the project team as needed.
  • Provide team leadership in specifically defined areas on behalf of the Project Leader.
  • Update and customize systems, tools, and project plans according to applicable standard operating procedures; support vendor selection; create project-specific training curricula; review time booking and analyze overconsumption with Functional Lead input for Project Leader review; suggest and follow through on actions to reduce overconsumption; review plans with the Project Leader and Finance Business Partner; review pass-through costs; support timely invoicing; coordinate with the Trial Master File lead, IPO, and eCBL on Trial Master File and site-payment setup; coordinate system-access setup with the Project Data Coordinator; ensure resources are requested in line with project scope and support resource escalations; and collect, distribute, and track insurance documents and Letters of Authorization.
  • Prepare and analyze study reports, highlight issues for the project team, and maintain systems and tools according to applicable standard operating procedures.
  • Provide team leadership while working with functions on Trial Master File compliance and investigator-payment oversight.
  • Maintain coherent project management plans and coordinate project activity planning and functional input; collaborate with the Project Leader and Functional Leads to execute the plans.
  • Review time booking and overconsumption, review pass-through costs, review project-specific training compliance and follow up on noncompliance, and assist with preparation and follow-up for Project Operational Review meetings.
  • Provide reports, metrics, and analysis to support Project Leader decisions, client reporting, and risk management; oversee project system access and ensure timely access reviews; and provide delegated oversight of defined project management areas on behalf of the Project Leader.
  • Prepare for and attend project meetings, support preparation of information for internal and client meetings, report on owned responsibilities, and track and follow up on action items through completion.
  • Collaborate with Project Leaders and Functional Leads to ensure study supplies are delivered as required and in accordance with contract obligations.
  • Review vendor invoices and follow up with vendors on invoice questions and queries.
  • Drive timely operational project closeout using the closeout checklist and communication with functions; collaborate with the Project Leader to close systems, archive documents, hand over final work to the sponsor, and support financial closeout.
  • Support the Clinical Operations Leader with responsibilities involving Clinical Trial Management System compliance; track and analyze site newsletters, site staff lists, shipment reports, laboratory reports, site contact reports, site closure activities, vendor reports, query reports, and other delegated reports.
  • When assigned, train and mentor new starters on systems and tools, provide feedback to the PS/PL Super User on Clinical Research Services technology and processes, and present topics and expertise at local and global department meetings.

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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