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

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
Key skills that make candidates successful in FSP roles

Teaser label

Industry

Content type

Blogs

Publish 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

In this blog, we outline the key skills and attributes that help professionals thrive in FSP environments and build long term careers in sponsor-embedded roles.

Read more
Headshot of female
From Lab Bench to Program Leadership: Sinéad McKeon's Career at ICON

Teaser label

Our People

Content type

Blogs

Publish 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

Teaser label

Discover how a career can evolve from hands on lab work to program management in this interview with Sinéad McKeon.

Read more
View all

Similar jobs at ICON

Senior Clinical Research Associate

Salary

Location

Malaysia, Kuala Lumpur

Location

Kuala Lumpur

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions

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

JR140427

Expiry date

01/01/0001

Leslie Garcia

Author

Leslie Garcia
Read more Shortlist Save this role
Analytical Monitor (advanced level)

Salary

Location

India, Bangalore

Location

Bangalore

Bengaluru

Remote Working

Hybrid

Business Area

ICON Strategic Solutions

Job Categories

Clinical Data Management

Job Type

Permanent

Description

We are currently seeking an Analytical Monitor (advanced level) to join our dynamic and expanding client-dedicated Integrated Data Analytics & Reporting team. In this role, you will play a pivotal pa

Reference

JR140695

Expiry date

01/01/0001

Abhisikta Mishra Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Italy, Milan

Department

Clinical Monitoring

Real World Solutions

Location

Milan

Remote Working

Remote 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) and CRA II's to join our diverse and dynamic ICON Biotech team. As a CRA at ICON, you will play a critical role in overseeing and ma

Reference

JR146456

Expiry date

01/01/0001

Sophie Bingham Read more Shortlist Save this role
Informed Consent Specialist

Salary

Location

India, Bangalore

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We're currently seeking an Informed Consent Form (ICF) Specialist to join our diverse and dynamic team. As an ICF Specialist at ICON, you'll be crucial in ensuring the accuracy, compliance, and timely

Reference

JR146421

Expiry date

01/01/0001

Kashifa Tahseen Read more Shortlist Save this role
PK Scientist

Salary

Location

UK, Reading

Location

Paris

Frankfurt

Dublin

Warsaw

Johannesburg

Bangalore

Reading

Bengaluru

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

Niki Scotto

Author

Niki Scotto
Niki Scotto

Author

Niki Scotto
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above