JUMP TO CONTENT

Project Manager, PCS

JR066928

About the role

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

Project Manager - Linguistic Validation

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

To be responsible for the coordination, execution, control and completion of single service projects ensuring consistency with ICON SOPs, service-line best practices, project contracts and budgets

  • In this role you will be in charge of managing Linguistic Validation and electronic implementation projects.

    Co-ordination of the assignment of suppliers who participate to linguistic validation projects.

    Co-ordination and management of multilingual translation projects responsible for ensuring that budget, deadlines and quality are met. Organize, animate and regularly monitor the work produced by members of internal and external project teams (based around the world).

The role

  • Primary point of contact for designated complex, single service projects and responsible for developing successful working relationships with clients (internal and external), and ensure repeat business return to ICON

  • Responsible for project scheduling and implementation, resource requirements and deliverables

  • Develop and maintain project management plans

  • Responsible for risk mitigation strategies, associated action plan and issue resolution

  • Responsible for managing cross-functional project team

  • Provide direction and support to project team

  • Manage projects in accordance with the contract budget and contracts

  • Collaborate with Client Services to ensure successful completion of change orders

  • Managing relevant invoicing procedures and revenue recognition, as needed

  • Track project deliverables using appropriate tools

  • Effectively monitor and report on progress of the project to all stakeholders

  • Implement QC activities as necessary and monitor relevant quality metrics

What you need

  • Minimum of Bachelor's Degree or local equivalent (Language/Translations preferred)

  • Experience in project management within the medical/pharmaceutical industry or translation agencies required

  • 3+ Project Management experience in the CRO, translation agencies, pharmaceutical, or biotechnology sector

  • Experience in managing large-scale, global projects mandatory

  • Demonstrate decisiveness in resolving business problems, making decisions and identifying priorities

  • Interpersonal skills to influence and spur change, facilitate and enhance performance within a cross - functional environment

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

Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
Female using a laptop to search for jobs
Improving Your Visibility in the Clinical Research Job Market

Teaser label

Career Progression

Content type

Blogs

Publish date

11/26/2025

Summary

How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por

Teaser label

Discover the search terms recruiters use most often and practical steps that can help candidates strengthen their visibility.

Read more
View all

Similar jobs at ICON

CTA

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Strategic Solutions

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

JR139999

Expiry date

01/01/0001

Ana Tello

Author

Ana Tello
Ana Tello

Author

Ana Tello
Read more Shortlist Save this role
Clinical Trial Liaison

Salary

Location

Miami, FL

Location

Jacksonville, FL

Miami, FL

Tampa, FL

Orlando, FL

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Liasion

Job Type

Permanent

Description

The Clinical Trial Liaison (CTL) will develop relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in pharmaceutical industry clinical trials f

Reference

JR137051

Expiry date

01/01/0001

Muna Nelke

Author

Muna Nelke
Muna Nelke

Author

Muna Nelke
Read more Shortlist Save this role
Quality Assurance Auditor II

Salary

Location

US, New York, NY, Whitesboro

Department

Full Service - Quality Assurance

Location

Whitesboro

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Quality Assurance

Job Type

Permanent

Description

We are currently seeking a Quality Assurance Auditor II to join our diverse and dynamic team at our bioanalytical lab in Whitesboro NY. As a Quality Assurance Auditor II at ICON, you will play a pivot

Reference

JR137508

Expiry date

01/01/0001

Muna Nelke

Author

Muna Nelke
Muna Nelke

Author

Muna Nelke
Read more Shortlist Save this role
Medical Imaging Data Analyst I

Salary

Location

Mexico, Mexico City

Department

Full Service - Development & Commercialisation Solutions

Location

Mexico City

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Analyst

Job Type

Permanent

Description

Medical Imaging - Data Analyst I Mexico City - Based at office with Flex: 3 Days at Office and 2 days at homeWhat You Will Be Doing:Primary responsibilities include management of data analysis and dat

Reference

JR139194

Expiry date

01/01/0001

Daniela Guerrero Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

UK, Reading

Location

Reading

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

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, you will play a critical role in overseeing and managing clinical tri

Reference

JR138809

Expiry date

01/01/0001

Sophie Bingham Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Romania, Bucharest

Location

Bucharest

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking experienced Clinical Research Associates with previous experience in oncology to join our diverse and dynamic FSP team in Romania.As a Clinical Research Associate at ICON Plc,

Reference

JR139956

Expiry date

01/01/0001

Dariusz Sternlicht Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above