JUMP TO CONTENT

Sr Dir, Stat Programming

044087_2

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.

List #1

Day in the life

Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
Female using a laptop to search for jobs
Improving Your Visibility in the Clinical Research Job Market

Teaser label

Career Progression

Content type

Blogs

Publish date

11/26/2025

Summary

How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por

Teaser label

Discover the search terms recruiters use most often and practical steps that can help candidates strengthen their visibility.

Read more
View all

Similar jobs at ICON

Clinical Research Associate

Salary

Location

United States of America

Location

Multiple US Locations

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. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical

Reference

JR140081

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Senior Medical Writer

Salary

Location

France, Paris

Location

Paris

Barcelona

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Medical Writing

Job Type

Permanent

Description

We are currently seeking a Senior OR Principal Medical Writer to join our diverse and dynamic team. As a Senior or Principal Medical Writer at ICON, you will be responsible for leading the development

Reference

JR137814

Expiry date

01/01/0001

Natalia Roth

Author

Natalia Roth
Read more Shortlist Save this role
Global Study Manager (Oncology/Hematology Cell Therapy)

Salary

Location

Canada, Burlington

Location

Montreal

Toronto

Burlington

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

What you will be doing: • Contribute to the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance. • Lead the preparation of country

Reference

JR140422

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Senior Specialist Publications Operations

Salary

Location

UK, Reading

Location

Warsaw

Madrid

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

The Senior Specialist Publications Operations is responsible for the execution of assigned medical, scientific and technical publications included in global disease publication plans. The manager will

Reference

JR137722

Expiry date

01/01/0001

Rajvir Samra

Author

Rajvir Samra
Read more Shortlist Save this role
Patient Recruitment Lead

Salary

Location

UK, Reading

Location

Reading

Swansea

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Patient Recruitment

Job Type

Permanent

Description

We have an incredible opportunity for a Digital Media Buyer to join ICON’s Patient Recruitment Solutions (PRS) digital team. The Digital Media Buyer is responsible for digital advertising material and

Reference

JR136129

Expiry date

01/01/0001

Rowena Deswert Read more Shortlist Save this role
Clinical Registry Administrator

Salary

Location

UK, Reading

Location

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Medical Writing

Job Type

Permanent

Description

As a Clinical Registry Administrator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Provides cli

Reference

JR138889

Expiry date

01/01/0001

Rajvir Samra

Author

Rajvir Samra
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above