JUMP TO CONTENT

Study Delivery Specialist

  1. Sofia, Prague, Budapest, Warsaw, Bucharest
JR144667
  1. Clinical Trial Support
  2. ICON Strategic Solutions (FSP)
  3. Remote or Office

About the role

Study Delivery Specialist

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Global Project Delivery role responsible for supporting end-to-end clinical study operations across international, multi-country trials. Partner closely with Study Managers and cross-functional teams to ensure studies are delivered efficiently, compliantly, and on schedule from study start-up through closeout and archival. The role involves coordinating global study activities, maintaining operational systems and documentation, overseeing vendors and CROs, tracking study performance, managing risks and budgets, and ensuring inspection readiness across all phases of clinical trials. Previous global project delivery experience within clinical research is mandatory.

Key Responsibilities
- Support full clinical trial lifecycle activities from study start-up through closeout and archival.
- Maintain and ensure accuracy of study systems, databases, trackers, and project plans.
- Collaborate with internal teams, CROs, and vendors to ensure compliant and efficient study execution.
- Monitor study timelines, quality, risks, budgets, and operational performance metrics.
- Review and contribute to critical study documents, including protocols, informed consent forms, and operational plans.
- Lead development and maintenance of study management plans such as monitoring, risk management, communication, and vendor management plans.
- Manage vendor and CRO relationships, oversee deliverables, and ensure delegated activities are completed on time.
- Provide country-level operational oversight including enrollment tracking, compliance, regulatory approvals, and issue management.
- Coordinate study meetings, maintain documentation repositories, track action items, and support team communications.
- Oversee clinical supplies and investigational product distribution while identifying and mitigating operational risks.
- Ensure inspection readiness through effective eTMF oversight and document quality management.
- Track study budgets, expenses, reconciliations, and change orders, escalating discrepancies when needed.
- Participate in cross-functional study teams and support adherence to company SOPs, regulations, and industry standard

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? Please click here to apply

List #1

Day in the life

A picture of chemists on a superimposed periodic table
5 reasons why you should consider a career in Clinical Research

Teaser label

Inside ICON

Content type

Blogs

Publish date

01/17/2025

Summary

Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities tha

Teaser label

If you’re seeking a rewarding and fulfilling work environment, a career at a CRO might be the perfect fit.

Read more
Man with headphones on looking at a laptop
Tips to make a lasting impression in a video interview

Teaser label

Career Progression

Content type

Blogs

Publish date

05/10/2024

Summary

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video

Teaser label

Ace your virtual job interview with these proven video interview tips.

Read more
A person using a pipette
Eliminating outsourcing confusion with ICON's new framework

Teaser label

Inside ICON

Content type

Blogs

Publish date

01/26/2023

Summary

The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials a

Teaser label

The CRO market has seen an unmistakable uplift in demand for its services in recent years.

Read more
View all

Similar jobs at ICON

Clinical Trial Associate

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a

Reference

JR141941

Expiry date

01/01/0001

Persis Davis

Author

Persis Davis
Read more Shortlist Save this role
CSS Standard

Salary

Location

China, Beijing

Location

Beijing

Guangzhou

Shanghai

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments an

Reference

JR152913

Expiry date

01/01/0001

Jenny Zhang

Author

Jenny Zhang
Jenny Zhang

Author

Jenny Zhang
Read more Shortlist Save this role
Clinical trial associate

Salary

Location

Spain, Barcelona

Location

Barcelona

Remote Working

Hybrid

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments an

Reference

JR153142

Expiry date

01/01/0001

Ana Guerra Garaeta Read more Shortlist Save this role
Clinical Trial Assistant

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.What You Will Do:You will take responsibil

Reference

JR152233

Expiry date

01/01/0001

Simone Chan

Author

Simone Chan
Simone Chan

Author

Simone Chan
Read more Shortlist Save this role
Clinical Trial Associate

Salary

Location

UK, Reading

Location

Reading

Cambridge

Remote Working

Hybrid

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are hiring a Clinical Trial Associate to start immediately or with 1 month notice maximum to join our dedicated team in Cambridge (England/UK).You will have the opportunity to join a well-establish

Reference

JR153048

Expiry date

01/01/0001

Elisabeth Trivic Read more Shortlist Save this role
Clinical Site Associate

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

As a Clinical Site Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and

Reference

JR149382

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above