Find jobs
Pricing
Sign in
FIND JOBSPRICINGSIGN INSIGN UP
← Back
IC
Icon

Project Manager, PCS

Location2 Locations
Work modeon-site
Typefull-time
DepartmentProject Management
Company size10,000+ people
First seen1w ago
Last seen1d ago
About the role
Project Manager, PCS - Mexico and Brazil
About the company
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Location: Brazil or Mexico
ICON Insights Evidence & Value (IEV) is part of ICON plc, a leading global Clinical Research Organization headquartered in Dublin, Ireland. Our group undertakes consultancy projects for international clients in both the pharmaceutical and medical device sectors, supporting late-phase clinical trials. The Project Manager will work on multiple projects focusing across different areas from market access, health economics, epidemiology & data analytics, health technology assessment & value communications and Patient Reported Outcomes. Our team is based in several countries such as US, UK, Brazil, Canada, Germany, France, Spain.
Role overview:
Responsibilities
As a Project Manager you will be expected to contribute towards a culture of business excellence with a focus on quality, scope, timelines adding value to the business and exceeding client expectations. You will be involved at the forefront of innovation and drive delivery using your project leadership expertise. Delivering successful working relationships with clients, cross functional project planning, scheduling, and implementation, defining project scope, resource requirements and deliverables, risk mitigation strategies, associated action plan and issue resolution and budget management.
You will also work in matrix teams on global international projects and be responsible for the overall coordination, implementation, and completion of regional/global cross functional projects, as well as provide expert project management input into new business proposals and bid-defence meetings.
What you will need:
•
3-5 years’ work experience within a CRO, central laboratory environment OR extensive clinical laboratory experience
•
Have a Degree in a Life Sciences, HEOR, Epidemiology, Business, Statistics, Economics, Project Management or related discipline
•
Strong communication, planning, decision-making, negotiation, conflict management and time management skills
•
Customer focussed with the ability to build excellent rapport with business partners
•
Comfortable with presenting to internal groups and external clients
•
Highly organised and remains calm in taking care of multiple priorities and working to tight deadlines
•
Passionate about developing a career within Project Management.
•
Passionate about Process Improvement and looking for ways to increase project management efficiencies
Skills
Nice to have
•
Fluency in English both orally and in writing, with excellent communication skills
•
Quality and detail-oriented
•
Strong organization and multitasking skills
•
Strong team player in a multi-cultural environment
•
Master-level skills in MS Word, PowerPoint and Excel
•
Proven ability in project planning, resource and risk management
•
Ability to tailor project planning tools to meet client needs and research (or project) strategy
•
Demonstrable ability to work independently and lead complex projects
•
Ability to clearly present instructions, negotiate pricing and address issues with suppliers and internal and external stakeholders on a global scale
•
Proven ability to work in a fast-paced environment and to work autonomously and manage aggressive delivery schedules
•
Anticipate and respond to client and/or project needs without prompting
•
Ability to identify action necessary to achieve goals and targets
•
Consistently reliable in delivering time sensitive demands and ongoing commitments with minimal supervision
•
Understanding of the pharmaceutical, biotech and medical device industry
•
Knowledge of IRB/Ethics committees
•
Knowledge of data privacy, transparency/Sunshine Act
•
Knowledge of Standard Operating Procedure (SOP)
•
Understanding of different project management methodologies i.e. Agile vs PMBoK
#LI-DG1
Legal
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
•
Competitive base salary and performance related incentives
•
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
•
Retirement and pension plans
•
Life assurance and disability coverage
•
Employee assistance programmes and wellbeing resources
•
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
More roles at Icon
Clinical Trial ManagerClinical Trial ManagerClient Contract Analyst II, Early PhaseClinical Site Associate(Senior) Clinical Research Associate
Seekless
Product
Find jobsCompaniesPricing
Legal
PrivacyTermsCookies
© 2026 SEEKLESS, INC. ALL RIGHTS RESERVED.BUILT WITH CARE