Global Contract Strategist

hace 4 semanas


Ciudad de México, Ciudad de México IQVIA A tiempo completo

Job Overview

IQVIA is seeking a skilled Contract Negotiator to develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs.

Key Responsibilities

  • Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.
  • Develop contract language, payment language and budget templates as applicable to the position.
  • Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan.
  • Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
  • Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
  • Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.

Requirements

  • Bachelor's Degree in a related field.
  • 3 years of relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator.

Equivalent combination of education, training and experience.

Desirable Skills

  • 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 the regulated clinical trial environment and knowledge of the drug development process.


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