Sr. Site Contracts Associate, Iqvia Biotech

IQVIA

São Paulo, Brazil
Negotiating clinical site contracts
Budget templates
Contracting strategy development
Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements

Job Summary

  • Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements.
  • 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.
  • Mentor and coach colleagues as required including the delivery of training materials as required.

Matching Summary

Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements.

Skills & Requirements

Must-have

  • negotiating clinical site contracts
  • budget templates
  • contracting strategy development
  • investigator grants and estimates
  • GCP/ICH and applicable regulatory guidelines

Nice-to-have

  • agile, therapeutically aligned solutions
  • trusted partnerships
  • breakthrough treatments to patients faster
  • collaboration with sponsors and stakeholders

Key Requirements

  • 3-5 years experience
  • Bachelor's Degree Related field
  • demonstrable global and/or regional experience
  • Good negotiating and communication skills
  • Strong legal, financial and/or technical writing skills
  • Strong understanding of regulated clinical trial environment
  • Knowledge of applicable regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter