Назад
Company hidden
6 дней назад

Senior Manager, Investigator Grants (Clinical Trials)

121 800 - 152 200$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Manager, Investigator Grants (Clinical Trials): Leading global investigator grant operations and CTMS-based site payment processing with an accent on payment accuracy, financial controls, reconciliations, and client reporting. Focus on implementing the CTMS Site Payment Module, configuring clinical trial payment terms, analyzing accruals and forecasts, and managing a global grants team.

Location: Remote, United States

Salary: USD 121,800–152,200 annually, plus eligibility for a discretionary annual bonus.

Company

hirify.global provides clinical solutions and supports clinical trial operations, including investigator site payment administration.

What you will do

  • Lead the global grants team responsible for accurate and timely investigator site payments through the CTMS.
  • Serve as the financial lead for site payments, including advance reconciliations, month-end reporting, projections, and key performance indicators.
  • Lead implementation of the CTMS Site Payment Module, including data validation, system setup, training materials, and transition of payment processing.
  • Configure and maintain global site payment terms based on Clinical Trial Agreements and ensure appropriate review, approval, and internal controls.
  • Partner with Project Directors and Project Managers to interpret financial terms, capture payment-eligible activities, and provide training.
  • Lead client meetings covering investigator grant results, accruals, forecasting, change order budgets, Sunshine Act reporting, and related reporting.

Requirements

  • Bachelor’s degree in business administration, accounting, finance, or a similar field.
  • At least 5 years of CRO experience or equivalent relevant experience and/or demonstrated competency in the key requirements of the role.
  • At least 3 years of experience managing direct reports.
  • Experience implementing a site payment module within a Clinical Trial Management System, including data validation, system setup, and user training.
  • Experience with international clinical trial payment processes, Clinical Trial Agreements, site budgets, grant administration, and site contracting.
  • Strong understanding of study start-up, financial analysis, reconciliation, reporting, time management, communication, and interpersonal collaboration.
  • Ability to work independently and in a team, manage multiple assignments, learn quickly, and improve processes while strengthening internal controls.

Nice to have

  • Experience with Veeva Vault CTMS.

Culture & Benefits

  • Remote work arrangement for the United States.
  • Health insurance, retirement savings benefits, life insurance, disability benefits, parental leave, and paid sick and vacation leave.
  • Eligibility for a discretionary annual bonus.
  • Work involves global collaboration with clients, investigator sites, project teams, and personnel across the organization.

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