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Worldwide Clinical Trials logo — Worldwide Clinical Trials Clinical Payments Specialist at Worldwide Clinical Trials
Worldwide Clinical Trials

Clinical Payments Specialist

Job · Full-timeWork from HomeIndia2-3 years1 opening

About this role

Worldwide Clinical Trials is hiring for Clinical Payments Specialist in India (Remote). This opening was published by Worldwide Clinical Trials on their official careers board (Workday) on 3 September 2026 and was confirmed live on 14 September 2026. Job details • Company: Worldwide Clinical…

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Skills you'll use

ExcelGCPProject ManagementCommunicationCustomer Service

What you'll do

  • _Tasks may include but are not limited to:_
  • Responsibilities include end to end management of global Investigator payments for assigned studies including:
  • Collection of information from all teams/systems/tools wherever needed on a timely and proactive basis
  • Understand global contract terms, budgets and payment schedules, ensuring that payments to investigative sites are aligned with the Clinical Trial Agreement.
  • Analysis and presentation of data in a required fashion to various stakeholders
  • Act as a Channel between the Sites/Clinical research teams interacting with the sites and other functional Leaders
  • Perform payment reconciliations at mandated intervals.
  • Complete analysis of budgeted versus actual spend for assigned projects and any other reporting needs as required. Review and discuss with project team.
  • Develop and provide budgetary forecasts for project teams for investigator payments
  • Develop and distribute consolidated monthly payments reports detailing the status of paid/unpaid sites in assigned study (s)

Who can apply

  • Excellent written and verbal communication skills
  • Ability to work independently and as a team member
  • Strong interpersonal skills in a fast-paced and rapidly changing environment
  • Ability to exercise independent judgment with sensitivity to decisions requiring supervisory approval
  • 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
  • Advanced skills in MS Office applications including Microsoft Word, Access, Excel, PowerPoint and Publisher.
  • Knowledge and understanding of ICH, GCP and FDA or EU directive regulations (as applicable) as well as local regulatory requirements
  • Excellent spoken and written English skills as well as fluency of the language of the country of location
  • Energetic, diligent, customer-oriented

About Worldwide Clinical Trials

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and…

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