Director Project Management Central Labs
About the role
This vacancy has now expired. Please click here to view live vacancies.
Director Project Management ICON Central Labs
Dublin, Ireland
This is an exciting opportunity to work within a fast paced environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Director, Project Management plays a key role within ICON Laboratory Services (ILS) by ensuring client satisfaction by acting as the main contact for all Project Management's Managers and Team Leads in all matters regarding ICL. Responsibilities include: proactive client care and partnership with key clients; providing direction of the Project Management Teams toward better internal and external customer satisfaction through early intervention, early risk assessments and voice of the customer realization; and finally assuring that the PM group is managing studies in accordance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Guidances.
Overview of the Role
- Work with key clients to understand current and upcoming needs in order to plan internal resource needs, enhance and re-direct services as needed, and drive improvements to our services and deliverables best suited to the client, always with a view to fostering the lab-client partnership.
- Review client metrics, including identifying areas of potential improvements or optimizations as needed by the PM Managers and Team Leads; delegate the investigation and troubleshooting of quality issues from internally or externally driven complaints and/or client audits.
- Prepare for and attend regular client meetings at a governance and operational management level to represent all of ILS and bring issues, concerns and future development needs back into ILS for consideration and implementation; Attends regular Protocol Review Committee meetings for capabilities considerations and for resource planning purposes; Involvement in Proposal Updates.
- Work with the BD Team and key Clients directly to build stronger relationships through listening to the voice of the customer at the client as well as communicating these needs to internal ILS interdepartmental service providers.
- Act as the PM Managers' or Team Leads' main contact / mentor / coach and the person to contact for all escalated matters regarding our central laboratory services. This will be accomplished by following up and responding to clinical study specific inquiries from both intra and inter departmental groups to provide further troubleshooting solutions and earlier proposal intervention and early risk assessments to minimize these through process improvements.
- Work with other internal groups to enhance interdepartmental interactions, such as having more involvement in new lab Implementation & training to explain what this means to clinical studies and therefore to our clients.
- Work with CRS to better align our services and to provide cross function ICON enhancements for our clients to choose from
- Performs additional relevant responsibilities as requested by management.
Authority
- Access to all active and closed projects to obtain big picture view of our service levels.
- Ability to attend all client meetings with internal parties
- Communication with internal and external vendors as required by job functions
- Advocate for the client with all internal departments to drive process improvement
- Issue escalation to Senior Management as appropriate.
- Manage all staff under his/her jurisdiction.
Supervision
- Ensure all necessary training is provided to his/her staff to improve their job performance and knowledge
- Proactively participate in the selection and recruitment of suitable and qualified staff
- Act as mentor/role model for Project Management / Team Leads
- Evaluate performance of direct reports.
- Support direct reports in establishing and accomplishing mutually agreeable goals that contribute to the success of the organization as a whole.
Role Requirements
- Hold a BS or BA in a Life Science or related field.
- Previous experience in clinical lab/ clinical trial , project management or related experience
- Previous line management experience
- Significant sponsor experience preferred.
- Must have a track record of successfully managing large/complex global programs.
- Strong history of success in building client relationships and client retention experience.
- Good understanding of project management processes and highly developed problem solving skills and knowledge of systems required for study management
- Significant leadership and well developed managerial skills with experience in client and internal presentations.
- Ability to oversee all aspects of project management and client relationship management, successfully manage PM Managers, interact positively with all levels of internal staff.
- Excellent oral and written communication skills.
- Experienced multi-tasker with the ability to work independently with a high degree of quality.
- Must be self-motivated with an outgoing personality and work well in a team setting
- Proven track record in delivering focused customer service and client satisfaction
- Proven ability to proactively manage a broad variety of clinical studies
- Experience in managing projects and/or client relationship management
- Strong history of success in building client relationships and client retention experience
- Capable of quickly building good rapport with clients, assessing their needs and presenting features and benefits of ILS's products and services
- Group presentation skills a plus
- Proven ability to utilize resources and successfully navigate an organization
- Knowledge and familiarity with the clinical trials industry
- Ability to effectively apply learned principles to broader situations
- Skilled in projecting and monitoring trends and performing risk management
- Ability to remain composed and even-keeled in stressful situations, performing effectively in spite of shifting priorities, workload and external pressures
- Accomplished as an action-oriented self-starter, actively seeking out self-improvement with a view to global thinking and team development.
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. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
06/06/2025
Summary
Building Connections that Drive Progress In an industry where collaboration is critical to advancing science and improving patient outcomes, networking is more than a professional courtesy - it’s
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/29/2025
Summary
Blood Cancer Day Blood Cancer Day is a powerful reminder of the millions of individuals and families whose lives are affected by hematological malignancies every year. These diseases are complex,
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/22/2025
Summary
World Schizophrenia Awareness Day 2025 Every year on 24 May, World Schizophrenia Awareness Day offers a vital opportunity to raise awareness, dismantle stigma, and celebrate the strength of individ
Similar jobs at ICON
Salary
Location
Toronto
Department
Clinical Monitoring
Location
Toronto
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119945
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Brazil, Mexico
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Brazil
Mexico
Business Area
ICON Strategic Solutions
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Senior Manager, Pharmacovigilance to join our diverse and dynamic team. As the Senior Manager in this role at ICON, you will be responsible for overseeing pharmacovigilance
Reference
2025-120086
Expiry date
01/01/0001
Salary
Location
Romania, Bucharest
Department
Clinical Monitoring
Location
Bucharest
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in desig
Reference
JR131574
Expiry date
01/01/0001
Author
Tereza SvobodovaAuthor
Tereza SvobodovaSalary
Location
France
Department
Clinical Trial Management
Location
France
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are constantly looking for motivated, reliable and dedicated CTMs who can demonstrate a first similar experience as a Clinical Trial Manager, Local Trial Manager or Study Manager within the pharmac
Reference
2025-119638
Expiry date
01/01/0001
Author
Katrien DoomsAuthor
Katrien DoomsSalary
Location
Poland
Department
Clinical Monitoring
Location
Poland
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2025-120093
Expiry date
01/01/0001
Author
Michal CzyrekAuthor
Michal CzyrekSalary
Location
Bulgaria
Department
Clinical Operations Roles
Location
Bulgaria
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119880
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz Sternlicht