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

Headshot image of male
Driving Trials Forward: Study Start-Up Leadership at ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/16/2026

Summary

Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

Teaser label

Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

Read more
Male and female in lab
Who’s Who in a Clinical Trial Team

Teaser label

Inside ICON

Content type

Blogs

Publish date

03/15/2026

Summary

Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

Teaser label

Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

Read more
Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish 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

Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

Read more
View all

Similar jobs at ICON

Clinical Research Coordinator I

Salary

Location

Argentina, Buenos Aires

Location

Buenos Aires

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Research Site Services

Job Type

Contractor

Description

We are currently seeking a fixed term - part time CRC Level 1 to join our diverse and dynamic team. As a CRC Level 1 at ICON, you will play a pivotal role in designing and analyzing clinical trials, i

Reference

JR143063

Expiry date

01/01/0001

Florencia  Borello Taiana Read more Shortlist Save this role
Global Study Lead

Salary

Location

United States of America

Location

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Global Study Lead to join our diverse and dynamic team. As the Global Study Lead, you will hold a crucial role in ensuring the successful delivery of all clinical aspects of

Reference

JR147353

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Senior Clinical System Designer- Electronic Health Data

Salary

Location

Ireland, Dublin

Location

Dublin

Johannesburg

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Systems

Job Type

Permanent

Description

Do you have experience in creating building Rave studies, creating data transfer agreements, data mapping? Are you looking to work with Electronic Health Records and be involved in a new exciting role

Reference

JR144620

Expiry date

01/01/0001

Rowena Deswert Read more Shortlist Save this role
Senior PK Scientist

Salary

Location

UK, Livingston

Location

Paris

Dublin

Milan

Madrid

Mechelen

Assen

Livingston

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Pharmacokenetics

Job Type

Permanent

Description

We are seeking an experienced Clinical Pharmacology professional to support protocol development and pharmacokinetic/pharmacodynamic (PK/PD) analysis across Phase I–IV clinical trials as Senior PK Sci

Reference

JR146673

Expiry date

01/01/0001

Rowena Deswert Read more Shortlist Save this role
PK Scientist

Salary

Location

UK, Reading

Location

Paris

Frankfurt

Dublin

Warsaw

Johannesburg

Reading

Assen

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Pharmacokenetics

Job Type

Permanent

Description

We are seeking an experienced Clinical Pharmacology professional to support protocol development and pharmacokinetic/pharmacodynamic (PK/PD) analysis across Phase I–IV clinical trials as PK Scientist.

Reference

JR146214

Expiry date

01/01/0001

Rowena Deswert Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above