JUMP TO CONTENT

Project Coordinator

JR074084

About the role

This vacancy has now expired. Please click here to view live vacancies.

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

Summary

The Bioanalytical Project Coordinator provides administrative support to the Bioanalytical Study staff for pre-clinical and clinical studies. This includes, but it not limited to, project related support by creating database designs supporting small or large global projects with low complexity; ensuring database set up according to standard operating procedures, policies, and good practice; and compiling project data tables according to client data agreements.

Responsibilities

  • Assist in set-up activities for the bioanalytical LIMS database design in support of clinical or preclinical protocols and protocol amendments.
  • Carry out all activities according to the appropriate ICON IBL SOPs, Good Clinical Practice (GCP), and Good Laboratory Practice (GLP).
  • Ensure that systems (e.g., GlobalBioA, Watson LIMS, etc.) are updated accordingly.
  • To facilitate production and documentation of presentations and organize team/customer meetings, finalizing minutes in collaboration with Bioanalytical Project Leader.
  • Will support project timelines as defined by the Bioanalytical Project Leader.
  • Assist in data management including processing, reviewing and creating data tables.
  • Ensures the delivery of high quality work to internal and external clients.
  • Maintain accurate project documentation.
  • Participate in audits, as required.
  • Assist in tracking and resolution of deviations as it pertains to study samples freezer storage pursuant to ICON IBL SOPs.
  • Provide sample coordination and administration including sample reconciliation.
  • Work closely with external customers to test data transfers and report results to Bioanalytical Project Leader.
  • Provide administrative support regarding data retrieval and delivery (via email and portals).
  • Ensure all requisitions and invoices are coded correctly to ensure costs are billed to the project or passed through to the client.
  • May provide back-up support on behalf of colleagues who are absent from the office.
  • Perform other duties as assigned by management.

Required Knowledge, Skills and Abilities

  • Strong verbal and written communication skills (including good command of the English language), telephone manner, team working skills, flexible attitude to work.
  • Ability to achieve results through collaborative efforts with others.
  • Good organizational, time management, and operational skills.
  • Good accuracy and attention to detail skills.
  • Ability to effectively balance multiple concurrent priorities.
  • Able to use initiative, plan ahead, proactive in problem solving, diplomatic and able to demonstrate appropriate decisions within scope of authority.
  • Ability to interact with external and internal clients, and work to objectives/timelines.
  • Ability to follow verbally communicated procedures.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  • Computer proficiency of Word, PowerPoint and Excel.
  • Desired knowledge of routine laboratory procedures.
  • Demonstrated ability to work in a fast-paced, high stress environment highly desirable.

Minimum Required Education and Experience

College degree and 1-2 years' relevant experience; or equivalent combination of education, training and experience. Bachelor's Degree in a scientific field preferred.

Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and 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 through the form below.

List #1

Day in the life

Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

Teaser label

Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

Read more
Headshot of female
From Lab Bench to Program Leadership: Sinéad McKeon's Career at ICON

Teaser label

Our People

Content type

Blogs

Publish date

02/05/2026

Summary

Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab

Teaser label

Discover how a career can evolve from hands on lab work to program management in this interview with Sinéad McKeon.

Read more
Headshot image of male
Shaping the Future of Patient Safety: A Conversation with Hassan Aljobori

Teaser label

Our People

Content type

Blogs

Publish date

02/05/2026

Summary

Shaping the Future of Patient Safety At ICON, patient safety is the foundation of everything we do. Hassan Aljobori, Director of Pharmacovigilance, shares his journey through nine years of growth

Teaser label

Hassan shares his career journey, advice for building a career in pharmacovigilance, and what sets ICON apart as an employer.

Read more
View all

Similar jobs at ICON

Site Contracts Negotiator II

Salary

Location

Mexico, Mexico City

Location

Mexico City

Multiple US Locations

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Contracts Administration

Job Type

Permanent

Description

We are currently seeking a Site Contracts Negotiator II to join our diverse and dynamic team. As a Site Contracts Negotiator II at ICON, you will independently manage the negotiation and execution of

Reference

JR139641

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
Senior CRA

Salary

Location

US, Blue Bell (ICON)

Department

Clinical Monitoring

Location

Blue Bell

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal

Reference

JR145426

Expiry date

01/01/0001

Jasmine Garcia Read more Shortlist Save this role
Senior Study Start-up Associate

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Senior Study Start Up Associate to join our diverse and dynamic team. As a Senior Study Start Up Associate at ICON, you will be working within a large-scale, fast-paced envi

Reference

JR145168

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Sr Clinical Research Coordinator - (Vaccine & Internal Med)

Salary

Location

US, Cary, NC

Department

Accellacare Site Network

Location

Cary

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Research In-Home Services

Clinic

Job Type

Permanent

Description

This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site net

Reference

JR142126

Expiry date

01/01/0001

Sasha Brown

Author

Sasha Brown
Sasha Brown

Author

Sasha Brown
Read more Shortlist Save this role
Senior Manager, Site Identification

Salary

Location

US, Blue Bell (ICON)

Department

Accellacare Site Network

Location

Blue Bell

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site net

Reference

JR139212

Expiry date

01/01/0001

Sasha Brown

Author

Sasha Brown
Sasha Brown

Author

Sasha Brown
Read more Shortlist Save this role
Clinical Site Manager II (Sr CRA)

Salary

Location

Spain, Madrid

Location

Madrid

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical

Reference

JR145265

Expiry date

01/01/0001

Lola Pombo

Author

Lola Pombo
Lola Pombo

Author

Lola Pombo
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above