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 Budget Analyst - Vendor

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Accounting & Finance

Job Type

Permanent

Description

We are currently seeking an Clinical Budget Analyst (Vendor) to join our diverse and dynamic team. As a Vendor CBA at ICON, you will play a pivotal role in determining fair market value pricing for in

Reference

JR140441

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Freelance Senior CRA

Salary

Location

Australia, Melbourne

Department

Clinical Monitoring

Real World Solutions

Location

Melbourne

Sydney

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Contractor

Description

Role: Freelance Senior CRALocation: Sydney or MelbourneWe 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 p

Reference

JR139246

Expiry date

01/01/0001

Krisztina Auth Read more Shortlist Save this role
Clinical Data Risk Analyst

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Job Type

Permanent

Description

We are currently seeking a Clinical Data Risk Analyst to join our diverse and dynamic team. As a Clinical Data Risk Analyst at ICON, you will play a crucial role in identifying and mitigating risks as

Reference

JR136188

Expiry date

01/01/0001

Florencia  Borello Taiana Read more Shortlist Save this role
Clinical Trial Manager

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

Role : Clinical Trial ManagerLocation : Sao Paulo, BrazilWe are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsi

Reference

JR140560

Expiry date

01/01/0001

Elizabeth Davies Read more Shortlist Save this role
TMF Lead

Salary

Location

Mexico, Mexico City

Department

Full Service - Clinical Operations

Location

Mexico City

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Regulatory Document Management

Job Type

Permanent

Description

Role : Trial Master File LeadLocation: Mexico (Homebased)We are currently seeking a Trial Master File Lead to join our diverse and dynamic team. As a TMF Lead at ICON, you will be responsible for over

Reference

JR138837

Expiry date

01/01/0001

Elizabeth Davies Read more Shortlist Save this role
Manager Clinical Operations

Salary

Location

Greece, Athens

Department

Clinical Monitoring

Location

Athens

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Operations Management

Job Type

Permanent

Description

We are currently seeking a Manager, Clinical Operations to join our diverse and dynamic team. As a Manager, Clinical Operations at ICON, you will play a pivotal role in overseeing the execution of cli

Reference

JR140302

Expiry date

01/01/0001

Lourdes Roy Prats Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above