Sr Dir, Stat Programming
Hi, I am Kellyand I manage this role
Talent Acquisition Specialist
About the role
This vacancy has now expired. Please click here to view live vacancies.
The global senior director of programming will lead and set the strategic direction of the global programming group and drive the successful implementation of the strategy. S/he will lead a culture that will lead to growing and scalable statistical programming capabilities. This will be an inspirational leadership role that will make a compelling case for change and lead through example with an engagement in delivering profitable growth and business operational efficiencies.
The Senior Programming Director will perform this role by;
· Establishing & drive business strategy
· Leading & driving the execution of business initiatives
· Evaluating initiative impact on the organization
· Drive the delivery of studies activities which exceed client expectation
· Lead the creation and improvement of internal procedures, focused on process improvement to add value to ICON’s business and meet client needs
· Provide change leadership and lead projects to drive standardization, stability and simplification in processes
· Establish and maintain effective working relationships with sponsors and internal departments/business units
· Ensure appropriate participation in preparation of costings, proposals and bid defence meetings
· Maintain professional expertise and position of respect amongst peers
· Ensure department managers monitor individual project/programs and resourcing to ensure revenue targets and margins are achieved
· Direct line management responsibility for individuals including managers within the department, including setting global focus, goals, processes and objectives
· Recruit, train, develop and appraise management personnel
· Travel will be around 10-15%.
Role Requirements
- Degree (BSc/MS/PhD) in statistics, biostatistics, mathematics, computer science, or related field
- Significant clinical research experience, specifically in the pharmaceutical industry, including previous line management responsibility
- Demonstrable ability to direct programming initiatives, with statistical programming experience including analysis data sets, tables, listings and graphs
- Excellent organizational, planning and problem solving skills
- Excellent oral and written communication skills with the ability to interface at all levels both internally and externally
We are a company of 13,500 employees in forty countries globally. We differentiate ourselves by developing innovative solutions to bring life-saving drugs to market faster and in a more cost-effective way to foster better patient outcomes. We are a top five clinical research organization with solid earnings and growth potential. Our belief in excellence is our core value in all that we do for our sponsor partners and the patients that we serve. As a company we strive to exceed our customers’ expectations in drug development solutions.
Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent retirement plan, health coverage, paid time off, income protection insurance programs, and staff recognition schemes. We care about our people, since 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. Caring for patients while enjoying what we do and delivering great results is something we can achieve if we know we can count on each other and have a clear vision of where we want to go.
ICON is an equal opportunity employer – Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
Teaser label
IndustryContent type
BlogsPublish date
10/28/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
Similar jobs at ICON
Salary
Location
United States of America
Location
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
This role involves supporting the execution of clinical trials by managing administrative tasks and monitoring trial progress. The position is responsible for coordinating and tracking all study docum
Reference
JR139022
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
Japan, Tokyo
Location
Tokyo
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Corporate Support
Job Type
Permanent
Description
【職務内容】弊社のFSP部門(Functional Service Provider)における外部就労案件にてBusiness Operations Manager – Site Contracting(弊社タイトルManager, Contracts想定)として下記ご担当いただきます。※ご経験によっては、Business Operations Associate - Site Contracti
Reference
JR137772
Expiry date
01/01/0001
Author
Mai TakanashiAuthor
Mai TakanashiSalary
Location
US, Lenexa KCIB (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Lenexa
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical & Scientific Affairs
Job Type
Temporary Employee
Description
We are currently seeking an Environmental, Health & Safety (EHS) Manager to join our diverse and dynamic team. As an EHS Manager at ICON, you will play a pivotal role in ensuring the safety and well-b
Reference
JR139106
Expiry date
01/01/0001
Author
Hanna PitcairnAuthor
Hanna PitcairnSalary
Location
Mexico, Mexico City
Department
Full Service - Medical Affairs & Pharmacovigilance
Location
Mexico City
Sofia
Warsaw
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Operations
Pharmacovigilance & Patient Safety
Job Type
Permanent
Description
What you will be doing: Conduct comprehensive reviews of clinical trial protocols, patient records, and medical documentation to ensure compliance with study protocols and regulatory requirements.Coll
Reference
JR138500
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR138529
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna DuarteSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Senior Regulatory TechnicianLocation: Mexico City only – Office based role (Hybrid)As a Senior Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also
Reference
JR134308
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth Davies