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Site Activation Lead

168 ICON Clinical Research Poland sp. z.o.o. · Warsaw, Poland

Clinical TrialsLeadExternal listingfull-time22 days ago

About The Role

Site Activation Lead - Europe - homebased

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

At ICON, study start-up is not a checklist — it’s the moment where strategy becomes access. As a Site Activation Lead , you ensure clinical trials move from plan to reality without unnecessary delays, protecting timelines, budgets, and most importantly — patient access to new therapies.

This role is about ownership, impact, and performance.

What You’ll Be Responsible For — and Why It Matters

  • Design and lead Study Start-Up Plans - So that every country and site moves forward with clarity, alignment, and realistic timelines.
  • Drive regulatory and ethics submissions to approval - So studies reach activation faster and without avoidable rework or compliance risk.
  • Oversee site contracts and budget negotiations - So financial and legal barriers don’t delay first patient in.
  • Identify risks early and implement mitigation strategies - So roadblocks are prevented — not reacted to.
  • Partner with sponsors at Bid Defences and Kick-Off Meetings - So start-up strategy is strong from day one and aligned with expectations.
  • Lead and empower regional start-up teams - So performance is consistent, accountable, and milestone-driven across countries.
  • Ensure data accuracy, reporting, and KPI tracking - So sponsors have transparency and projects stay on course.

Every action you take directly influences time-to-activation — and ultimately, time-to-treatment for patients.

What You Bring

  • 5+ years in Clinical Research with strong Study Start-Up experience
  • Deep understanding of regulatory frameworks and submission processes
  • Proven ability to lead cross-functional teams globally
  • Strong project management and risk mitigation skills
  • Confidence in sponsor-facing environments

#LI-MK1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways
  • Benefits may vary depending on role and location.
  • Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

  • ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
  • If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .
  • Are you a current ICON Employee? Please click here to apply

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