Senior Site Feasibility Specialist – Iqvia Biotech, Poland

IQVIA

Warsaw, Poland
Base: 102.800,00 zł - 272.500,00 zł; bonus/equity:...
Site activation activities
Regulatory documents accuracy
Clinical systems understanding
Lead country-level Site Activation (SA) activities, ensuring timely start-up of investigative sites in alignment with global and local regulations, SOPs, and project objectives

Job Summary

  • Lead country-level Site Activation (SA) activities, ensuring timely start-up of investigative sites in alignment with global and local regulations, SOPs, and project objectives.
  • Serve as the Single Point of Contact (SPOC) for assigned studies, working closely with investigative sites, Site Activation Managers (SAMs), Project Management, and cross-functional partners.
  • Join a mission-driven organization dedicated to improving patient outcomes through innovative clinical research and work in an agile environment with the support of global resources.

Matching Summary

Lead country-level Site Activation (SA) activities, ensuring timely start-up of investigative sites in alignment with global and local regulations, SOPs, and project objectives.

Salary

Base: 102.800,00 zł - 272.500,00 zł; Bonus/Equity: Not specified; Benefits: health and welfare and/or other benefits

Skills & Requirements

Must-have

  • Site Activation activities
  • regulatory documents accuracy
  • clinical systems understanding
  • GCP/ICH guidelines knowledge
  • drug development process familiarity

Nice-to-have

  • negotiation and communication skills
  • organizational and prioritization skills
  • relationship building skills

Key Requirements

  • Minimum 3 years clinical research experience
  • At least 1 year leadership capacity
  • Bachelor’s degree Life Sciences or related field
  • Local and international regulatory requirements understanding

Work Rights

Not specified

Tailored Resume

Cover Letter