Senior Site Contracts Specialist — Remote

Worldwide Clinical Trials Holdings, Inc.

United States

À distance

USD 90 000 - 130 000

Plein temps

Il y a 12 jours
Générateur de candidature

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Résumé du poste

Worldwide Clinical Trials Holdings, Inc. in the United States is seeking a Senior Site Contracts Specialist to lead the end-to-end management of clinical trial agreements. You will act as SME on CTA processes at country and site levels, ensuring compliance and competitive budgets across global sites.

The role requires negotiating complex contracts, preparing site budgets, and coordinating with sponsors, investigators, and cross-functional teams to finalize documents with accuracy.

Qualifications

  • 3-4 years as Senior Site Contracts Specialist or minimum 5 years Site Contract experience in Clinical Research Pharmaceutical or CRO industry
  • Bachelor's Degree or equivalent in business administration, finance, law, science or related field
  • Proficiency with MS Word, Excel and Outlook

Responsabilités

  • Act as a SME on Clinical Trial Agreement processes at country and site level
  • Preparation, negotiation and finalization of site contracts and budgets
  • Manage the Investigator Budget and act as a key liason for contract related communications
  • Resolve negotiation issues and escalating risks, drive process for improvements, contribute to SOP develoment and keep templates updated
  • Liaising and collaborating with Worldwide stakeholders as well as external stakeholders (such as sites, investigators etc.)
  • Review and finalize Clinical Trial Agreements and/or any document associated including site budget, for completeness and accuracy

Connaissances

Contract negotiation
Contract drafting
Regulatory knowledge
Communication
Cross-functional collaboration

Formation

Bachelor's Degree or equivalent

Outils

MS Word
MS Excel
Outlook

Description du poste

Worldwide Clinical Trials Holdings, Inc. in the United States is seeking a Senior Site Contracts Specialist to lead the end-to-end management of clinical trial agreements. You will act as SME on CTA processes at country and site levels, ensuring compliance and competitive budgets across global sites.

The role requires negotiating complex contracts, preparing site budgets, and coordinating with sponsors, investigators, and cross-functional teams to finalize documents with accuracy.

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