Associate Project Leader - Medical Communications
TA Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please click here to view live vacancies.
Associate Project Leader - Medical Communications
At ICON, it's our people set us apart.
ICON Global Medical Communications combines strategic consulting with delivery of innovative, insightful, and impactful tactics to optimise communication of your product's clinical value to a variety of external stakeholders.
We aim to be the best strategic medical communications company and scientific content partner in the world. We have committed ourselves to achieving this mission by leading the industry in quality, service, and innovation…Would you like to join our team?
We are looking for passionate, resilient, and inspiring individuals to join our team. As the Associate Project Lead, you are responsible for day-to-day project management of multiple assigned clients including the resourcing, execution, management, financial oversight, and delivery of sold client work with Access, Commericalization and Communications business units.
The role
- Chair and manage regular status meetings among internal stakeholders
- Ensure financial trackers are kept up to date for ICON and client purposes (monthly and weekly)
- Ensure clients are billed accurately and in a timely manner
- With support, manages projects in a timely manner in adherence with SOPs and appropriate guidelines as necessary.
- Leads the development and maintenance of project management documents, including but not limited to, project timelines, project management plans, communication plans and risk analysis plans.
- Liaises appropriately with internal functional leads and clients on project related matters.
- Keeps management informed of project status in relation to quality, timelines and staff issues.
- Liaise with rest of project management group to ensure appropriate staffing throughout project lifecycle. Monitor project staff allocation in appropriate resource management system(s).
- Communicates effectively with others at all levels within the organization and with clients/vendors.
- Works in collaboration with internal and external colleagues to meet project objectives, timelines, and budget.
- Follows and contributes to departmental and corporate policies and procedures.
- Takes responsibility for project tasks and sees them through to successful completion.
- Completes special projects and miscellaneous assignments as needed to meet project and/or departmental objectives.
- Participation in Lunch and Learns or other internal company training sessions.
- Supports development and tracking of goals, budget and other financial metrics
- Supports identification and implementation of process improvement initiatives as appropriate.
- Manage technical and administrative functions for multiple, simultaneous, complex projects.
- Ensures project activities are consistent with project requirements and contractual scope of work.
- Ability to recognize and mitigate risk, creatively problem solve, and effectively crisis manage multiple projects in a fast-paced agency environment
- Able to adapt to changes in deadlines and changes in the nature of assignments.
- Able to appropriately prioritize competing project demands.
- Preferably makes appropriate use of available technology and tools in seeking and implementing solutions.
- Capable of seeking and implementing standard and alternative solutions to problems.
- Works well with other individuals and departments to solve problems.
- Consistently produce high-quality work.
What you need
- A minimum of a Bachelor's degree or local equivalent
- Prior Pharma Agency experience (preferably in Medical Communications)
- Minimum of 1-2 years of experience in related field
- Strong communication skills written and orally
- Strong computer skills, sound knowledge of MS Office Suite and Adobe Acrobat
- Ability to multi-task, support various projects
Why join us?
Ongoing development is vital to us, and as an Associate Project Lead, you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.
EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin
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
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
Teaser label
Our PeopleContent type
BlogsPublish date
03/24/2026
Summary
Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv
Teaser label
Our PeopleContent type
BlogsPublish date
03/16/2026
Summary
Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl
Similar jobs at ICON
Salary
Location
Poland, Warsaw
Department
Full Service - Corporate Support
Location
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
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
JR148168
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Poland, Warsaw
Location
Sofia
Prague
Budapest
Dublin
Riga
Warsaw
Lisbon
Bucharest
Belgrade
Barcelona
Madrid
Bratislava
Reading
Tbilisi
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Project Management
Job Type
Permanent
Description
About the roleAt ICON plc, we are committed to improving and saving lives through clinical research. As a Project Manager – Feasibility & Site Activation, you will play a critical role in driving the
Reference
JR148219
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Site Specialist I (Study Start Up Associate I) to join our diverse and dynamic team. As a Site Specialist I at ICON, you will support investigator sites with key administrat
Reference
JR146306
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
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
JR144856
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Poland, Warsaw
Location
Sofia
Warsaw
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Pharmacovigilance Assistant II to join our diverse and dynamic team. As a Pharmacovigilance Assistant II at ICON, you will play a critical role in ensuring the accurate coll
Reference
JR145206
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
US, San Antonio, TX, ICR
Location
San Antonio
Lawrence
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Liaison
Job Type
Permanent
Description
ICON’s field-based Clinical Trial Liaisons are highly trained site engagement specialists who support clinical trials by providing scientific and clinical support to investigators and site staff to en
Reference
JR145932
Expiry date
01/01/0001
Author
Muna NelkeAuthor
Muna Nelke