IQVIA Biotech is seeking a Senior Site Feasibility Specialist in Poland to lead site activation activities for clinical studies. The role involves serving as a key liaison among various stakeholders to ensure compliance with regulations and timely project execution
Job Summary
The role involves leading country-level Site Activation activities to ensure timely start-up of investigative sites in alignment with global regulations.
Candidates will serve as the Single Point of Contact for assigned studies, working closely with investigative sites, internal teams, and sponsors.
IQVIA Biotech offers an agile environment with support from global resources and opportunities for career growth while improving patient outcomes.
Matching Summary
Match Score: 85
IQVIA Biotech is seeking a Senior Site Feasibility Specialist in Poland to lead site activation activities for clinical studies. The role involves serving as a key liaison among various stakeholders to ensure compliance with regulations and timely project execution.
Salary
Base: 102.800,00 zł - 272.500,00 zł; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare benefits included
Skills & Requirements
Must-have
Site Activation management
Regulatory document preparation
GCP/ICH guidelines knowledge
Investigative site liaison
Project timeline planning
Nice-to-have
Strong negotiation skills
Effective cross-functional collaboration
Ability to challenge when needed
Agile environment experience
Key Requirements
Bachelor's degree in Life Sciences or related field
Minimum 3 years of clinical research experience
At least 1 year in a leadership capacity
Knowledge of local and international clinical trial regulatory requirements