JUMP TO CONTENT

Sr Statistical Programmer I

040791_2

About the role

This vacancy has now expired. Please see similar roles below...

 
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior Statistical Programmers play a key role within ICON developing and executing statistical programs designed to analyze clinical trial information.
 
The Senior Statistical Programmer will be responsible for designing and developing standard software and data structures, developing and executing statistical programs designed to analyze clinical trial information and participating in the development and maintenance of SOPs (including software validation, documentation, study archiving and others as needed). The Senior Statistical Programmer will also be responsible for Leading programming deliverables and programming teams, effective resource planning, project tracking, ensuring project, timeline and quality goals are consistently achieved, effectively liaising with other functions in the conduct of programming activities, and also working in a sponsor facing lead role. This position can be based in the UK, Ireland or Central Europe, with potential for home-based working. 
 
Overview of the role
 
  • Develop and execute statistical analyses of clinical trial data. Design and develop computer programs that produce tables, figures, listings and derived datasets that summarize results of clinical trials.
  • Participate in the review of Case Report Forms (design phase), Statistical Analysis Plans, QC Specifications and Database Structures.
  • Assess data from clinical trials for consistency and accuracy.
  • Develop and implement quality assurance software.
  • Design and implement analysis file structures.
  • Monitor procedures for software validation.
  • Work on cross-disciplinary teams to assure programming needs are met and appropriate requests are made.
  • Leading programming deliverables and programming teams
  • Sponsor facing lead role
 
Role Requirements
 
  • Bachelors of Science degree in a quantitative discipline (or training equivalent to) or equivalent work experience.
  • 8+ years full time SAS programming experience for Senior Programmer; experience must be in the pharmaceutical or biotechnology industry.
  • Understanding of data structures, standard software and their implementation.
  • Knowledge of the drug development process (Phase I through IV) and general regulatory requirements.
  • Good written and verbal communications skills
  • Prior oncology experience preferable
 
If you are looking to join a company which will offer you a strong support network and an inspiring working environment, then this is the job for you.  Applicants must be able to demonstrate drive, passion and a strong sense of team working, along with a desire to progress within our organisation. Successful candidates will also have great communication, both verbal and written.
 
 
In return, we offer a strong benefits package that includes comprehensive health and pension plans, competitive salary, holidays, and an incentive plan for strong performers.
 *LI-AC1
List #1

Day in the life

Endometriosis yellow ribbon
Shining a Light on Endometriosis Awareness Month

Teaser label

Inside ICON

Content type

Blogs

Publish date

04/18/2024

Summary

Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis

Teaser label

Endometriosis Awareness Month sheds light on this often-misunderstood condition affecting millions worldwide.

Read more
Data visualisation
The Role of Data Management in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

04/18/2024

Summary

Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials

Teaser label

This blog examines the critical role of data management in clinical trials.

Read more
Medicine on a shelf
Navigating the Clinical Research Supply Chain

Teaser label

Industry

Content type

Blogs

Publish date

04/12/2024

Summary

Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ

Teaser label

Discover the intricate workings of the clinical research supply chain in this comprehensive guide.

Read more
View all

Who we are

Press play to find out more

Similar jobs at ICON

Clinical Research Coordinator Nurse

Salary

Location

US, Winston-Salem, NC 27103

Location

Winston-Salem

Business Area

ICON Full Service & Corporate Support

Job Categories

Nursing

Job Type

Contractor

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR118118

Expiry date

01/01/0001

Mitzi Overton

Author

Mitzi Overton
Read more Shortlist Save this role
Senior Clinical Research Coordinator

Salary

Location

US, Winston-Salem, NC 27103

Location

Winston-Salem

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Research In-Home Services

Clinic

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR117595

Expiry date

01/01/0001

Mitzi Overton

Author

Mitzi Overton
Read more Shortlist Save this role
Medical Communications/Publications Intern

Salary

Location

US, Blue Bell (ICON)

Department

Full Service - Development & Commercialisation Solutions

Location

Blue Bell

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Intern

Job Type

Intern

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It

Reference

JR116869

Expiry date

01/01/0001

Jasmine Garcia Read more Shortlist Save this role
Qualified Revenue Accountant

Salary

Location

Ireland, Dublin

Location

Dublin

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Accounting & Finance

Job Type

Permanent

Description

ICON PLC is currently recruiting for a Qualified Revenue Accountant to join our growing Order to Cash team, on a Permanent hybrid working basis at our Leopardstown HQ in Dublin.The Qualified Revenue A

Reference

JR114031

Expiry date

01/01/0001

Dimitri Bishop Malamos Read more Shortlist Save this role
In-House CRA

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

2024-109932

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Clinical Trial Assistant

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

2024-109898

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above