Investigator Payment Analyst 2 at IQVIA

Warsaw, Masovian Voivodeship, Poland

IQVIA Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, PharmaceuticalsIndustries

Requirements

  • Experience with site payment vendor management or oversight
  • Demonstrated ability of holding vendor accountable for services in Statement of Work (SOW)
  • Solid understanding of Fair Market Value benchmarks and assessments
  • Ability to manage global payments and total study budget, with specific emphasis on Poland
  • Experience with other country-specific payment rules and regulations
  • Experience in supporting R&D as it relates to Clinical Trial business operations
  • Ability to track and report on invoice aging and outstanding payments on a real-time basis
  • Oversight of invoice and payment status
  • Financial Acumen: Ability to perform predictive analysis utilizing enterprise and/or departmental tools and systems to forecast anticipated expenses
  • Solid understanding of variance analysis relating to budget vs actuals under site budget Purchase Orders
  • Solid understanding of Clinical Trial site budgets, contractual payment terms in executed Clinical Trial agreements and how they translate to payments to sites

Responsibilities

  • Support the Clinical Business Operations department and all studies in the Site Payment portfolio
  • Partner closely with investigative sites, the Clinical Operations team, Investigator Contracts Management team, Budget Development team, and site payment vendors
  • Apply critical and analytical thinking to the administration of accurate and timely site payments
  • Manage study portfolio by planning, executing, and tracking of global clinical trial payments
  • Implement the SOW and Change Order process and project related cost, if applicable
  • Assess project performance to monitor the progress of projects, identify and quantify variances, perform required corrective actions and communicate to all stakeholders
  • Successfully work with 3rd party site payment vendor to resolve site payment discrepancies, historical payment issues, and monthly reporting requests
  • Track payments owed to clinical research sites in accordance with the negotiated unit price per the site’s Contract
  • Perform risk mitigation actions to proactively oversee invoice review, approval, and payments
  • Support management in identification of risks, develop mitigation strategies, alternative solutions, resolve issues, action item/follow up in collaboration with cross functional and/or matrix teams and present to IPM management
  • Alignment with internal functional partners on invoice and payment related discussions prior to communication with external partners and/or investigative sites
  • Maintain frequent and consistent communication with external partners and/or investigators and internal departments regarding payment activities during the study lifecycle
  • Perform predictive analysis utilizing enterprise and/or departmental tools and systems to forecast anticipated expenses

Skills

Vendor Management
Statement of Work
Fair Market Value
Budget Management
Invoice Tracking
Predictive Analytics
Variance Analysis
Clinical Trial Agreements
Payment Oversight
Financial Forecasting

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.
Proliferation of disparate technological solutions causes technology overload in clinical trials.
Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.
The company offers privacy-enhancing technologies to protect individual patient data.
IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.
AI-driven drug discovery accelerates identification of potential drug candidates.
Expansion of telemedicine facilitates remote patient monitoring and data collection.

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