IQVIA logo
IQVIA

Accelerate innovation for a healthier world.

Senior Site Contract Associate – Biotech

Location

Spain

Posted

1 day ago

Salary

0

Seniority

Senior

Bachelor Degree6 yrs expEnglishGoogle Cloud Platform

Job Description

Senior Site Contract Associate – Biotech

IQVIA

• Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs • Develop simple investigator grant estimates and proposal text to support the proposal development process • Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials • Ensure collaboration with sponsors, stakeholders and RSU regions and countries • Provide specialist operational and financial contracting support • Assist in the creation and/or review of core scientific, technical and administrative documentation • Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence • Ensure overall contracting efficiency and adherence to project timelines and financial goals • Comply with contract management and quality standards • Provide administrative and operational support to investigator site contract analysts, managers and directors • Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans.

Job Requirements

  • Bachelor's Degree in life sciences or health care
  • +6 years relevant experience
  • Relevant sponsor or clinical research organization clinical site contracting experience
  • Good negotiating and communication skills
  • Good interpersonal skills and a strong team player
  • Strong technical writing skills
  • Understanding of regulated clinical trial environment and knowledge of drug development process
  • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
  • Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards
  • Good organizational and planning skills
  • Strong knowledge of Microsoft Office and e-mail applications
  • Ability to interpret pricing models and to prepare proposals, bid grids and budgets
  • Good understanding of clinical trial contract management.

Benefits

  • Health insurance
  • Flexible working hours
  • Professional development opportunities

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