Sr Facil & Admin Coordinator
About the role
This vacancy has now expired. Please click here to view live vacancies.
The Role:
At ICON Plc, we have an exciting opportunity for an expert Senior Facilities and Administration Coordinator to join our APAC team. This is an important role for us as you will work with business leaders to ensure that our Manila site is maintained to the highest standards.
Responsibilities:
Effectively coordinate the day to day administrative and facilities services in the office in compliance with departmental procedures in addition to general ICON procedures.
Oversee the preparation of financial information as required by local and company accountants, including invoice processing, CAPEX and lease approvals. Ensure completion of tasks within accounts cycle and resolve queries in a timely manner (where applicable).
Coordinate local use of the Facilities Online System, ensuring compliance with department metrics.
Coordinate sourcing and monitoring of suppliers, including ordering, stock control and distribution.
Management of suppliers including quality service checks, contract review and negotiation in compliance with QA guidelines and company policies.
Coordinate any building contract maintenance and repair including such services as heating, air conditioning, security systems, elevators, utilities and fire safety equipment (where applicable).
Coordinate Health & Safety Systems in the office. Act as local Health and Safety Officer or liaise with company Heath and Safety Officer to ensure local compliance with Health and Safety legislation. Ensure all Health and Safety documentation is up to date, that suitably trained Health and Safety representatives and fire wardens are available within the company (where applicable).
Management of departmental budget costs (where applicable).
Coordination and delivery of staff induction.
Company Mobile Phone Account management (where applicable) and Car Fleet Management (where applicable).
Management and distribution of in bound faxes both hardcopy and electronic (where applicable).
Physical resource coordination, including space allocation for workstations, cellular offices and meeting rooms.
Management of external records management & data security services (where applicable).
Support the IT function at a local level, assisting in setup and management of services for staff (where applicable).
Assist the HR function with recruitment process, maintenance of HR files, payroll tasks and management of PeopleSoft database (where applicable).
Keep management informed of any issues within the organization that require attention.
Perform other reasonably related duties as may be locally required.
Requirement:
Degree qualified ideally in relevant facilities & administration discipline.
Prior relevant experience in a Facilities and Administration related role in a large organisation.
Experience collaborating on larger facilities projects a distinct advantage.
Strong financial/accounting, budgetary, tracking and reporting experience.
Proficient with Microsoft Office Suite particularly Excel Experience working with AutoCAD & space planning an advantage.
Experience in specifying, costing and carrying our small to medium Facilities Projects.
Ability to be inventive and proactive in taking care of issues that may arise.
Strong oral and written communication skills, with proficiency in English.
Strong interpersonal skills and ability to interact at all levels.
Awareness of workplace Health & Safety regulations.
Benefits of Working at ICON:
Other than working with an outstanding team of ambitious people, we also offer a very competitive compensation package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our employees as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
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
IndustryContent type
BlogsPublish date
02/16/2026
Summary
What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh
Teaser label
IndustryContent type
BlogsPublish date
02/16/2026
Summary
Functional Service Provision (FSP), also known as sponsor-embedded delivery, is a core part of how modern clinical research is delivered. At ICON Strategic Solutions, our teams work as an extens
Teaser label
Our PeopleContent type
BlogsPublish date
02/05/2026
Summary
Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinica
Reference
JR146250
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
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 Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety
Reference
JR144856
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
US, Sherman Oaks, CA
Location
Los Angeles
Colorado
California
Arizona
Washington
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
We are seeking a Senior Clinical Site Lead to join a dynamic team working within the client environment.The candidate will be expected to travel to sites on the West Coast of the US. What you will be
Reference
JR145838
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
JR146216
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
Chicago, IL
Location
Indianapolis, IN
Chicago, IL
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit
Reference
JR146514
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
US, Raleigh, NC
Location
Raleigh
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit
Reference
JR146510
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon Pupek