Project Manager, PCS
Talent Acquisition Specialist
- Full Service Division
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.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish 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
Our PeopleContent type
BlogsPublish date
01/26/2026
Summary
Sometimes the best way to recognise what you have is to experience life without it. For Izabella Grimaldi, a Clinical Research Associate II based in Brazil, that realisation came after seven months wo
Teaser label
IndustryContent type
BlogsPublish date
01/20/2026
Summary
Understanding the Difference Between CRA, CTA, and SMA Clinical research job titles can be confusing, particularly for those new to the industry. Acronyms such as CRA, CTA and SMA appear frequentl
Similar jobs at ICON
Salary
Location
US, Blue Bell (ICON)
Location
Tennessee
North Carolina
Blue Bell
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Management
Job Type
Permanent
Description
We are currently seeking a Program Manager, Clinical Data Science to join our diverse and dynamic team. As a Program Manager in Clinical Data Science at ICON, you will play a crucial role in overseein
Reference
JR143178
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Regional Puerto Rico (PRA)
Location
Puerto Rico
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR142571
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
US, Blue Bell (ICON)
Location
Multiple US Locations
Blue Bell
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Patient Recruitment
Job Type
Permanent
Description
We have an incredible opportunity for a Digital Media Buyer to join ICON’s Patient Recruitment Solutions (PRS) digital team. The Digital Media Buyer is responsible for digital advertising deployment,
Reference
JR143656
Expiry date
01/01/0001
Author
Tallulah PierreAuthor
Tallulah PierreSalary
Location
US, Raleigh, NC
Location
Montreal
Raleigh
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Visualization Developer to join our diverse and dynamic team. As a Visualization Developer at ICON, you will play a pivotal role in programming (CDMS, data validation, data
Reference
JR143464
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and
Reference
JR143698
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
Mexico, Mexico City
Department
Full Service - Clinical Operations
Location
Mexico City
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
Role : Trial Master File LeadLocation: Mexico (Homebased)We are currently seeking a Trial Master File Lead to join our diverse and dynamic team. As a TMF Lead at ICON, you will be responsible for over
Reference
JR140438
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth Davies