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Site Budget and Contracts Specialist

hace 2 meses

Xico, México Iqvia Argentina A tiempo completo

Job Overview

The Site Budget and Contracts Specialist is a key member of our team at Iqvia Argentina, responsible for providing a suite of Site Budget and Contracts Services to our clients. This role will participate on a project team to deliver Site Budget and Contracts Services to a specific client on time, within budget, and in accordance with applicable financial, contractual, and pharmaceutical R&D industry standards and regulations.

Key Responsibilities

  • Serve as the client's primary point of contact for projects that utilize a single Site Budget and Contracts service for US and Canada.
  • Lead internal project kick-off meetings for single solution engagements, including a review of the Statement of Work (SoW) and the service delivery model that will be followed to execute the services.
  • Prepare Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), or other related contractual documents based on client-approved templates.
  • Negotiate contractual documents using the negotiation and escalation plan established with the client.
  • Track the delivery of services against the SoW and ensure that agreed-upon project targets and/or milestones are being achieved.
  • Lead client-specific or departmental projects, which may require oversight of other Site Budget and Contracts staff to ensure that these projects are delivered within established timelines.
  • Prepare ongoing unit-based forecasts for assigned projects and measure performance against those forecasts.
  • Serve as an internal escalation point for project-related issues and challenges.

Qualifications

  • Bachelor's Degree in a related field.
  • 5 years of relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator.
  • Experience supporting US and Canada site contracts is essential.
  • Good negotiating and communication skills, with the ability to challenge.
  • Good interpersonal skills and a strong team player.
  • Strong legal, financial, and/or technical writing skills.
  • Strong understanding of regulated clinical trial environments and knowledge of drug development processes.