Associate Centralized Monitoring Lead - Sponsor Dedicated, Poland (hybrid/home-based)

IQVIA UK

Poland
Base: zł102,800.00 - zł190,900.00; bonus/equity: n...
Hybrid/home-based
Centralized monitoring experience
Subject level data review
Ich gcp compliance knowledge
IQVIA UK is seeking an Associate Centralized Monitoring Lead to oversee centralized monitoring activities for clinical studies in Poland. The role involves ensuring compliance with regulatory requirements and quality standards, along with providing mentorship and support to clinical study teams

Job Summary

  • The role involves leading the execution of Centralized monitoring activities across multiple sites and studies from initiation to closeout while ensuring adherence to SOPs and Good Clinical Practices.
  • Candidates will be responsible for reviewing structured clinical data, performing subject-level data reviews, and managing site-level Key Risk Indicators (KRIs) to ensure data integrity and patient safety.
  • This position offers the opportunity to act as a subject matter expert, mentor central monitors, and contribute to process enhancements and automation initiatives within the clinical operations team.

Matching Summary

Match Score: 85

IQVIA UK is seeking an Associate Centralized Monitoring Lead to oversee centralized monitoring activities for clinical studies in Poland. The role involves ensuring compliance with regulatory requirements and quality standards, along with providing mentorship and support to clinical study teams.

Salary

Base: zł102,800.00 - zł190,900.00; Bonus/Equity: Not specified; Benefits: Health and welfare and/or other benefits

Skills & Requirements

Must-have

  • Centralized Monitoring experience
  • Subject Level Data Review
  • ICH GCP compliance knowledge
  • Risk-based quality management
  • Site Visit Report review
  • KRI and QTL analysis

Nice-to-have

  • Advanced analytics proposal development
  • Mentorship and coaching skills
  • Automation of ISP processes
  • Cross-cultural communication abilities
  • Strong presentation skills

Key Requirements

  • Bachelor's Degree in Clinical or Life Sciences
  • Minimum 3 years of relevant work experience
  • Minimum 1.5 years of Central Monitoring experience
  • Good Clinical system expertise
  • Strong written and verbal English communication skills

Work Rights

Not specified

Tailored Resume

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