Clinical Payments Specialist

Worldwide Clinical Trials; Tandil; Vor Ort; ARS 92.909.000 - 131.622.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking a Clinical Payments Specialist to manage end-to-end Investigator payments for global studies. The role requires coordination with sites, finance, and clinical teams to ensure timely and accurate payments, audits, and reporting.

The ideal candidate will have a four-year degree, strong English skills, and demonstrated experience in data entry/validation within finance or contracts, with advanced MS Office proficiency.

Qualifikationen

• Minimum four-year college degree or equivalent.
• Experience in data entry/validation in Finance, PM or Contracts.
• Excellent English, written and spoken.

Aufgaben

• End-to-end management of global Investigator payments for assigned studies.
• Set up, deployment, management and close-out of the study payments solution.
• Prepare consolidated monthly payment reports and forecasts.
• Conduct payment reconciliations and respond to inquiries from sites and sponsors.

Kenntnisse

Communication skills

Ausbildung

Four year college degree

Tools

MS Office Suite

Jobbeschreibung

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.
With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.

• SUMMARY: The Clinical Payments Specialist is a full-time position responsible for end to end management of global Investigator payments for assigned studies*.* The Clinical Payments Specialist **is responsible for the set-up, deployment, management and close-out of the study payments solution* *RESPONSIBILITIES: * _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) Participate in client, and project team meetings Prepare, participate in and follow up on audits / inspections Participate in all required applicable trainings Point contact for all Investigator related queries on assigned studies. Identify trends in underpayment/overpayments Evaluate trends and works towards resolution and improvement of revenue cycle processes Work with financial and clinical departments collaboratively Research and identify payment discrepancies from various sources Provide high level of customer service to both internal customers from the global WCT organisation and external sites and sponsors Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. *OTHER SKILLS AND ABILITIES: * 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 *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 Four year college curriculum or university degree OR Two year college curriculum and one or more years’ experience in office administration or similar position, OR Skill sets and proven performance equivalent to above English, written and spoken, advanced level Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.