**RESPONSIBILITIES**:- End to end management of global Investigator payments for assigned studies- Understand global contract terms, budgets and payment schedules, ensuring that payments to investigative sites are aligned with the Clinical Trial Agreement, perform payment reconciliations at mandated intervals- Complete analysis of budgeted versus actual spend for assigned projects and any other reporting needs as required- Develop and provide budgetary forecasts for project teams for investigator payments and develop and distribute consolidated monthly payments reports detailing the status of paid/unpaid sites in assigned study(s)- Prepare, participate in and follow up on audits / inspections**SKILLS**- Ability to work independently and as a team member- Strong interpersonal skills in a fast-paced and rapidly changing environment- Ability to handle multiple tasks, including rapid response in generating new documents, forms and tools- Strong organizational skills, including ability to develop naming conventions and filing architecture- Knowledge and understanding of ICH, GCP and FDA or EU directive regulations (as applicable) as well as local regulatory requirements- Energetic, diligent, customer-oriented**REQUIREMENTS**:- At least 2 years' experience with a CRO/Pharma Company in a relevant job involving qualitative data entry, data validation in Finance, Project Management or Contracts is preferred- Bachelor's/University degree or equivalent experience- English, written and spoken, advanced levelTipo de puesto: Tiempo completoSalario: $40,000.00 - $50,000.00 al mesHorario:- Lunes a viernes- Turno de 8 horasPrestaciones:- Seguro de gastos médicos mayores