Project Manager, IRT (Home-based)
About the role
This vacancy has now expired. Please click here to view live vacancies.
Position Summary:
Effectively manage and support moderate to complex IxRS activities of individual studies from award to closeout. This will include all non-technical Project Management activities including gathering of the client's system requirement, Scope/Budget control and System Maintenance. The project manager will be expected to interact and build relationships with both internal and external clients. Study implementations and support functions are cross functional and require problem solving across people and technology. Actively coach and mentor the Project Leaders and other junior staff on the Project Manager role and different tasks and responsibilities for that role. The Project Manager will manage studies based upon a monthly budget with full project support.
Job Responsibilities:
- Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
- Develop, support and manage projects and project plans for implementation and through life of the project.
- Develop system specifications requirements with the support of the Technical Project Manager while providing the client with solutions during design meetings.
- Develop and maintain project issues list and drive the issues to resolution.
- Maintain and present project metrics to project director and Sr. management.
- Provide coaching and personal development to project leaders and other junior staff.
- Maintain budget for all projects assigned. The project manager is responsible for carrying a minimum defined budget per month across projects allowing for one project in development phase to be managed.
- Schedule and facilitate meetings with clients to develop system requirements and maintain on-going project status meetings. Continuing to facilitate project status meetings and liaise with client during life of the project.
- Liaise with internal teams and clients to effectively manage scope changes, project budget/financials and service levels within a project.
- Adhere to all company and departmental procedures at all times.
- Comply with all company and departmental quality procedures, training and policies, and project and/or client defined service level agreements. Responsible for overall quality of the project.
- Be actively involved on process improvement activities within Project Management team.
- Manage project risks and manage risk mitigation activities independently while maintaining compliance with company and departmental procedures.
- Prepare and participate in bid defense meetings for new and existing clients.
Requirements:
-Bachelor's degree in life sciences, business, technology, information technology or related discipline or local equivalent or equivalent work experience
An alternative combination of experience, education and training determined by management to be equivalent to the foregoing
-Minimum 2 years' experience in clinical research OR IxRS services
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.
- Ability to produce high quality deliverables and work in an environment with changing priorities Understanding of system development life cycle process
- Negotiation skills, team work, conflict management, excellent leadership, documentation and communication skills, planning and organizing skills, effectively work with individuals across the organization, detail oriented
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
IndustryContent type
BlogsPublish date
04/03/2026
Summary
Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re
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
Similar jobs at ICON
Salary
Location
Bulgaria, Sofia
Location
Sofia
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Safety Scientist
Job Type
Permanent
Description
We are currently seeking a Principal Safety Scientist to join our diverse and dynamic team. As a Principal Safety Scientist at ICON, you will be responsible for leading safety assessments and pharmaco
Reference
JR148065
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
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
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
Norway,Oslo(KCR)
Location
Oslo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR147892
Expiry date
01/01/0001
Author
Keri MarshallAuthor
Keri MarshallSalary
Location
Bulgaria, Sofia
Location
Sofia
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
JR141803
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
Ireland, Dublin
Department
Full Service - Development & Commercialisation Solutions
Location
Dublin
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Supplies
Job Type
Permanent
Description
We are currently seeking a Global Supply Chain Specialist to join our diverse and dynamic team. As a Global Supply Chain Specialist at ICON, you will play a crucial role in managing and optimizing the
Reference
JR139602
Expiry date
01/01/0001
Author
James SmithAuthor
James SmithSalary
Location
Bulgaria, Sofia
Location
Sofia
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
As a Senior Global Regulatory Scientist at ICON, you will support the development, implementation, and execution of regulatory strategies for clinical development programmes.What You Will Do:You will
Reference
JR148452
Expiry date
01/01/0001
Author
Teodora KaykievaAuthor
Teodora Kaykieva