Operation Program Specialist
- Any EMEA Location
- Clinical Monitoring
- ICON Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Support a project and/or program(s) in the development and maintenance of program management tools, documents, plans, templates as well as the creation and tracking of program headcount, metrics, training and implementation of new processes.
Tracking and Metrics
- Assist in the creation of and maintenance of project management, program management and/or functional operational management templates, documents, tracking tools and databases.
- Run reports from PRA or client systems as needed to compile, provide first level review, and monitor performance metrics.
- Support collection and monitoring of project and/or program performance utilizing metrics data.
- Support collection and presentation of information for routine project and/or program review, functional operational review and quarterly executive review.
- Support the collection and maintenance of resource workload projections for overall project /program.
- Run utilization reports.
- Assist with collection and reporting of all project/program level metrics and KPIs, for example turnover, recruitment, and training metrics.
- Track team members start and stop dates, LOAs, and changes in title.
- Complete project/program level documentation for new hires and ends.
- Maintain personnel contact list and distribute to appropriate team members.
- Track various project and program related activities and documents such as project team calendars, monitoring.
- QC finance fee schedules or invoices to ensure accuracy from an operational perspective, including: headcount, function titles and assigned bill rates.
- QC new hire ERFs for accuracy and follow up on errors. Update ERFs as necessary.
Project/Program Support
- Assist with administrative tasks as assigned by the manager.
- Support set up and maintenance of SharePoint sites as needed.
- Develop, complete, maintain and distribute PTO calendars per client requirements.
- Synchronize management’s PRA and sponsor calendars.
- Schedule meetings, set up teleconference arrangements, invite attendees, create agendas, attend meetings and produce meeting minutes.
- Assist in preparation of regional meetings and events.
- Assist with the production of newsletters.
- Maintain required program/project documentation.
- Update program/project documentation as requested, including but not limited to: Relationship Management Plan, Communication Plan, Rules of Engagement, and Escalation Plan as requested.
- Provide administrative support to regional CRAs such as sending out study related documents and site correspondence.
- Assist with the coordination of program trainings and ensure proper documentation is submitted to both sponsor and PRA training departments.
Personnel Support
- Assist with administrative tasks as assigned by the manager.
- Develop customized tracking and approval procedures for both expense reports and timesheets of staff tailored to individual clients’ requirements.
- Track employees’ PTO requests.
- Review missing timesheet report on an ongoing basis and take corrective action if employees appear on the report.
- Review training reports to ensure staff complete all training requirements.
- Perform training on timesheet and expense reporting as necessary for new hires.
- Ensure new field staff complete mandatory sponsor and PRA GCP training within the required timeframe and track receipt of the certificate of program completion, as applicable.
- Assist with the on-boarding process, including processing of project/ program specific paperwork, coordination of activities, and hand-offs to others within the department.
- Assist PRA recruiters as required with the organization of candidate interview schedules (for PRA and sponsor).
- Organize travel needs of team as requested.
- An Associate’s or Bachelor’s degree or its international equivalent in health sciences or business, from an accredited institution, or equivalent work experience to successfully complete the activities.
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
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
.jpg)
Teaser label
Inside ICONContent type
BlogsPublish date
01/17/2025
Summary
Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities that are
.png)
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2024
Summary
How to Become a Clinical Research Associate: A Step-by-Step Guide The clinical research industry is projected to reach $52.0 billion by 2026, growing at an impressive rate of 5.6% annually. This
.jpg)
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv
Similar jobs at ICON
Salary
Location
United States
Department
Clinical Monitoring
Location
United States
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Reference
2025-119565
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Sofia
Department
Clinical Monitoring
Location
Sofia
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120038
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
US, Blue Bell (ICON)
Department
Clinical Monitoring
Location
Blue Bell
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 Senior Clinical Research Associate (CRA) or CRA II to join our diverse and dynamic team. As a Senior CRA/ CRA II at ICON Plc, you will play a critical role in overseeing and
Reference
JR129089
Expiry date
01/01/0001
Author
Zach HinesAuthor
Zach HinesSalary
Location
US, Downers Grove, IL
Location
Downers Grove
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical
Reference
JR130541
Expiry date
01/01/0001
Author
Zach HinesAuthor
Zach HinesSalary
Location
Poland
Department
Clinical Monitoring
Location
Poland
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
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
2025-119576
Expiry date
01/01/0001
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 Benner