Investigator Site Payments Analyst PCD

IQVIA; São Paulo; Teletrabalho; BRL 60 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Remote work

Resumo da oferta

IQVIA is seeking an enthusiastic associate to support clinical trials and payments with site networks as part of the FSP team. You will enable accurate and timely payment administration, adhering to SOPs and SLAs.

The role requires a bachelor’s degree, 1–3 years in pharma/clinical research, strong English communication, and the ability to work remotely within Brazil. Training and cross-functional collaboration are integral to the work.

Qualificações

• Bachelor’s degree in appropriate scientific or business disciplines.
• Excellent oral & written communication in English (advanced).
• 1–3 years of experience in pharmaceutical industry/clinical research.
• Home based role.
• Ability to work effectively in cross functional teams.
• Innovative spirit and ability to accomplish substantial tasks with minimal supervision.

Responsabilidades

• Manage a portfolio of projects and oversee the end-to-end process.
• Highlight aged invoices and financial risks and provide reasons for delays.
• Data quality control; ensure batches are scheduled per contracts and budgets.
• Perform project reconciliations and track KPI data for teams.
• Provide high level customer service to internal project teams and resolve issues.
• Check that appropriate approvals are obtained for setup and payment processes.

Conhecimentos

English proficiency

Analytical skills

Cross-functional teamwork

Problem solving

Formação académica

Bachelor’s degree

Ferramentas

MS Office

Descrição da oferta de emprego

We are looking for an enthusiastic associate interested in supporting clinical trials and payments activities with the sites, to join our FSP team.

Job Overview

You will provide support enabling the accurate and timely payment administration to our network of project sites. Perform duties in accordance with IQVIA Finance Standard Operating Procedures (SOPs), Sarbanes-Oxley Controls and Unit Service Level agreements (if applicable).

Essential Functions

• Managing a portfolio of projects and providing oversight on the entire process. Ability to form remote relationships with colleagues across the globe, consider indirect influences on your work and manage these.
• Highlighting aged invoices and financial risks – give reasons why for any delays.
• Data quality control, ensuring batches are scheduled as per contracts and meeting the budgets.
• Project reconciliations.
• Payment cycle target trending – ensuring the studies are meeting the target for each step in the payment cycle.
• Providing high level of customer service to internal project teams and assisting them in any project related issues by finding resolution. Ability to influence others and ensure that key actions are taken.
• Track and report metric data flagging nonstandard issues to project teams / line manager.
• Provide assistance to other team members as required, to ensure the group meets targets.
• Check that appropriate approvals are obtained for set up and payment process.
• Provide support and participate in teams handling various routine tasks.
• Provide standard reports and run KPI for the project teams.Perform other duties as assigned.
• File appropriate documents.

Education and Experience Requirements

• Graduated - Bachelor’s degree in appropriate scientific or business disciplines.
• Excellent oral & written communication in English (advance level).
• 1-3 years of experience and/or equivalent competencies in pharmaceutical industry/clinical research.
• Previous experience in systems would be an advantage however full training will be provided.
• Ability to work effectively in cross functional teams.
• Strong and proven analytical and problem resolution skills.
• Working knowledge of PCs (MS Office suite at a minimum).
• Must demonstrate innovative spirit and ability to accomplish substantial tasks with minimal supervision.
• Good written and oral communication skills as appropriate.
• Home based role.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Vaga Exclusiva para Pessoa com deficiência (PCD)