Global Program Lead - EU - Immunology
- Belgium, Germany, Spain, Switzerland, UK
- Project Management
- ICON Strategic Solutions (FSP)
Principal Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
We currently have an exciting opportunity to join ICON on an FSP program to a top global Pharma. The role is a Clinical Program Manager, permanent and home-based.
The Clinical Program Manager is a member of the core team for the drug development program, plays a key role in planning, executing, monitoring, reporting, controlling, and closing out projects and is accountable for the project time lines, budget and scope, the project risk management and scenario planning.
- Partners with the Global Program Head (GPH), Program Management Lead (PML) and the Global Program Team (GPT) members in the execution of Integrated Evidence plans and integrated program plan, achieving on-time or accelerated decision points and milestones. Manages cost, timelines, and quality of program and/or taskforce activities.
- Leads or assists with program quarterly budget Forecasts, and other budgeting activities.
- Supports GPH/PML with program communication coordination and ensures information flow within the GPT.
- Acts as an integrator to ensure alignment and leverage best practices, collaborate with team members to establish efficient processes within the GPT.
- Tracks and follows up on action items from team meetings and ensures project stakeholders are fully informed of team decisions.
- Functions as a change agent for continuous improvement and transformational initiative implementation within the GPT
- Depending on business needs, may be assigned as Global Program Manager or Regional Japan / China / India Program Manager
- Global Program Manager accountabilities
- Responsible for leading cross-functional program management activities for one or more life- cycle management Global Program Team (GPT) if applicable
- Leads taskforces or workstreams identified by PST/GPT to deliver quality results within agreed timeline.
- Accountable for cross-functional team meeting set-up, logistics and collaborating with GPH and/or PML on agenda/minutes. Develop and format PowerPoint slide decks, in partnership with the GPH and/or PML.
- Partners with the PML and/or GPH on communications including developing and maintaining SharePoint and Microsoft Teams collaboration sites, program level distribution lists, Team Roster, Action Items, Decision Log (or delegate to Program Coordinator if applicable)
- Supports GPH/PML to coordinate the set-up and logistics for program off-site meetings and events (PML/PM can delegate to Program Coordinator if applicable)
- Collaborates with GPT members to develop high-quality data packages for governance and committee interactions to enable fast decision-making if applicable.
- Accountable for the quality and accuracy of program-level data in the iMAP system in partnership with the Project Planner.
- For projects that are being jointly developed, work closely with alliance management to manage a key strategic alliance partner.
- Coordinates the process of updating program dashboard/reports.
- Connects RPM to GPT on regional topics if appropriate.
- Bachelor or Masters' degree in Life Sciences or other discipline related to drug development is required.
- Professional Project Management training, certification (e.g., PMI, IPMA) preferred.
- Approximately 5+ years of experience in drug development in the global pharmaceutical industry with approximately 3+ years of experience in project management
- Experience working in a global matrix team environment preferred.
- Strong written and verbal communication skills in English.
- Excellent technical skills in Microsoft Office (Word, Excel, PowerPoint, Teams, SharePoint).
- Appropriate leadership skills and ability to influence without authority with clear potential for leadership roles in the future.
- Mindset of results-orientation in collaborative setting
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
Career ProgressionContent type
BlogsPublish date
05/30/2023
Summary
Clinical research is the backbone of the life sciences industry. In fact, the established processes used to accurately trial and research medical, surgical and behavioural intervention are
Similar jobs at ICON
Salary
Location
US, Blue Bell (ICON)
Department
Full Service - Development & Commercialisation Solutions
Location
Raleigh
New York
Blue Bell
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Project Management
Project Management
Job Type
Permanent
Description
As a Senior Project Manager, Laboratory at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapie
Reference
JR151576
Expiry date
01/01/0001
Author
Frank LampartAuthor
Frank LampartSalary
Location
US, Blue Bell (ICON)
Department
Full Service - Development & Commercialisation Solutions
Location
Raleigh
New York
Blue Bell
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Project Management
Project Management
Job Type
Permanent
Description
Project Manager II, Laboratory- Farmingdale NY- Blue Bell PA- hybrid The Project Manager, Labs will ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Labo
Reference
JR150596
Expiry date
01/01/0001
Author
Frank LampartAuthor
Frank Lampart