JUMP TO CONTENT

Study Delivery Specialist

  1. Sofia, Vilnius, Warsaw
JR144245
  1. Clinical Trial Support
  2. ICON Strategic Solutions (FSP)
  3. Remote

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.

Study Delivery Specialist
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 standards
#LI-MC1

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

Team Lead, Site Operations

Salary

Location

US, Hickory, NC

Department

Accellacare Site Network

Location

Hickory

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We have an exciting opportunity for a Team Lead, Site Operations to join Accellacare in Hickory, NC. As a Team Lead, you will lead a team responsible for supporting site-facing activities across clini

Reference

JR145731

Expiry date

01/01/0001

Tallulah Pierre Read more Shortlist Save this role
Clinical Trial Associate

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Hybrid

Business Area

ICON Strategic Solutions (FSP)

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

JR152906

Expiry date

01/01/0001

Ana Tello

Author

Ana Tello
Ana Tello

Author

Ana Tello
Read more Shortlist Save this role
Global Study Associate

Salary

Location

South Africa, Johannesburg

Location

Johannesburg

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of opera

Reference

JR149853

Expiry date

01/01/0001

Shelley Ball

Author

Shelley Ball
Read more Shortlist Save this role
Site Management Associate II (Remote CRA II)

Salary

Location

Brazil, Sao Paulo

Department

Real World Solutions

Location

Sao Paulo

Mexico City

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Site Management Associate II to join our diverse and dynamic team. As a Site Management Associate II at ICON, you will play a vital role in supporting the management and mon

Reference

JR145326

Expiry date

01/01/0001

Diego  Tonini

Author

Diego Tonini
Read more Shortlist Save this role
Team Lead, Site Operations (Oncology)

Salary

Location

US, Downers Grove, IL

Department

Accellacare Site Network

Location

Downers Grove

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We have an exciting opportunity for a Team Lead, Site Operations to join ICON's Accellacare team. As a Team Lead, you will lead a team responsible for supporting site-facing activities across clinical

Reference

JR145498

Expiry date

01/01/0001

Tallulah Pierre Read more Shortlist Save this role
Clinical Trial Associate

Salary

Location

Israel, Tel Aviv

Location

Tel Aviv

Remote Working

Remote

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

JR150914

Expiry date

01/01/0001

Salome Kankia

Author

Salome Kankia
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above