~5d ago

Clinical Payments Specialist (LATAM)

2 Locationsmid

Other

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Quick Summary

Key Responsibilities

Collection of information from all teams/systems/tools wherever needed on a timely and proactive basis Understand global contract terms, budgets and payment schedules,

Technical Tools

Other

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 excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

Responsibilities

~1 min read

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

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