Global Study Manager

ICON Strategic Solutions

Polska

On-site

PLN 180,000 - 280,000

Full time

3 days ago
Be an early applicant
Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Benefits offered by this job

Competitive salary
Health insurance
Annual leave
Career development
Global exposure
Travel opportunities

Job summary

ICON Strategic Solutions seeks a Clinical Trial Manager to oversee day-to-day trial operations and ensure high-quality outcomes across our programmes. You will lead cross-functional teams, manage timelines and budgets, and drive study deliverables with a focus on compliance.

Travel to sites and investigators is expected (approximately 25%). The role offers exposure to global trials and a strategic impact on patient outcomes.

Qualifications

  • University degree in medicine, science, or equivalent combination of education & experience.
  • Demonstrated ability to drive the clinical deliverables of a study.
  • Subject matter expertise in the designated therapeutic area.
  • Prior monitoring experience is preferred.
  • Willingness to travel as required (approximately 25%)

Responsibilities

  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management
Team leadership
Stakeholder management
Regulatory compliance

Education

University degree in medicine or science

Job description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

What You Will Do

You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.

Key Responsibilities Include
  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Your Profile

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required Qualifications And Experience
  • University degree in medicine, science, or equivalent combination of education & experience
  • Demonstrated ability to drive the clinical deliverables of a study
  • Subject matter expertise in the designated therapeutic area
  • Prior monitoring experience is preferred
  • Willingness to travel as required (approximately 25%)
What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee?

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Global Study Manager
Global Study Manager

ICON Clinical Research • Polska

Hybrid
PLN 180,000 - 240,000
Annual leave entitlements
Health insurance
Retirement planning
+2
Clinical Trial Associate
Clinical Trial Associate

ICON Strategic Solutions • Warszawa

On-site
PLN 60,000 - 80,000
Annual leave
Health insurance
Retirement planning
+3
CRL Assistant
CRL Assistant

ICON • Warszawa

On-site
PLN 120,000 - 180,000
Annual leave
Health insurance
Retirement planning
+6
Study Site Management Specialist
Study Site Management Specialist

ICON Strategic Solutions • Polska

On-site
PLN 180,000 - 240,000
Annual leave
Health insurance
Retirement planning
+8
Clinical Trial Manager II
Clinical Trial Manager II

IRE • Poland

On-site
PLN 261,000 - 392,000
Health and wellbeing programs
Retirement and pension plans
Life assurance and disability coverage
+1
Site Engagement Study Manager
Site Engagement Study Manager

ICON • Warszawa

On-site
PLN 180,000 - 240,000
Annual leave entitlements
Health insurance
Retirement planning
+3
CTA (CSA)
CTA (CSA)

ICON Strategic Solutions • Poland

On-site
PLN 60,000 - 90,000
Annual leave
Health insurance
Retirement planning
+3
Site Activation Partner I
Site Activation Partner I

ICON Strategic Solutions • Polska

On-site
PLN 70,000 - 110,000
Health insurance
Annual leave
Retirement plan
+2
CRL Assistant
CRL Assistant

ICON Strategic Solutions • Poland

On-site
PLN 180,000 - 240,000
Annual leave entitlements
Health insurance
Retirement planning
+2
Clinical Supplies Project Manager
Clinical Supplies Project Manager

ICON Clinical Research • Poland

Remote
PLN 150,000 - 210,000
Annual leave entitlements
Health insurance offerings
Retirement planning offerings
+1