JUMP TO CONTENT

Prin Statistical Programmer

043684_2

About the role

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

"At ICON, it's our People that set us Apart"
 
 Are you interested in joining a respected Biostatistics and Programming team?
 
The Principal Statistical Programmer will be aligned to a project leadership or technical expertise role, encompassing the following responsibilities:-
 
Core responsibilities include:
  • Lead and execute programming deliverables on multiple projects in parallel and ensure that competing priorities are managed appropriately.
  • Lead and manage the assigned programming team’s deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines and to the highest standard of quality.
  • Proactively plan for and implement effective resource planning, task allocation and tracking of workload in accordance with agreed metrics (e.g. KPIs) and quality standards.
  • Serve in a client-facing capacity that demonstrates an ability to anticipate client needs and implement innovative solutions, as appropriate.
  • Develop and foster client relationships through effective project management and communication.
  • Apply exceptional technical capabilities and knowledge of industry trends to develop broad-use technical solutions for the benefit of study teams across the department.
  • Develop, implement and maintain documentation to technically train staff in the appropriate technical solution.
  • Actively participate in the review and approval of programming procedures and techniques.
 
Benefits of working at ICON:
 
ICON has a strong reputation for our approaches to clinical development.   We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients.   We help top pharmaceutical organizations across all phases of clinical development and many therapeutic areas to save lives and improve the quality of life.  We have a presence in over 40 countries, with over 80 offices 10,000 employees worldwide. 
 
In addition to partnering with the top pharmaceutical and biotech companies in the world, we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives.  
 
To succeed you will need:
 
  • Deliver high quality statistical programming deliverables for all assignments that consistently meets study timelines, quality standards, sponsor and/or contractual requirements.
  • Ensure high quality deliverables for assigned team members by performing quality control and review of programming outputs for accuracy and consistency.
  • Adhere to programming specifications and study specific requirements, including completion and filing of required documentation.
  • Plan, organize and prioritize workload to ensure effective time management and adherence to project specific timelines.
  • Efficient use of SAS, and adherence to SAS programming guidelines.
  • Create listing and safety outputs (analysis datasets, tables, figures) to a high standard of quality and accuracy.
  • Validate listing and safety outputs (analysis datasets, tables, figures) per departmental procedures.
  • Create efficacy outputs (analysis datasets, tables, figures) to a high standard of quality and accuracy.
  • Validate efficacy outputs (analysis datasets, tables, figures) per departmental procedures.
  • Create complex programs (such as project or departmental macros) to a high standard of quality and accuracy.
  • Validate complex programs (such as project or departmental macros) per departmental procedures.
  • Create analysis dataset specifications (ADaM or client-specific) to an exceptional standard of quality and accuracy.
  • Set-up standard programming directories and start-up utilities.
  • Create, document and validate project/study-macros at the table, listing and figure level.
  • Trouble-shoot and resolve programming issues in a timely and efficient manner.
  • Liaise effectively with other ICON functions (e.g., PM, DM, MW), as required during the life of the project.
 
US/LATAM/CAN:  A minimum of 8 years relevant experience of successfully performing the role of Statistical Programmer, preferably in the clinical research industry. Prior experience of successfully leading multiple projects in parallel or exceptional technical capability, including ability to develop broad-use technical solutions for the department.
 
Bachelor’s degree, in a quantitative or scientific discipline, or local equivalent.
 
 
We invite you to review our opportunities at www.iconplc.com/careers.
 
What’s Next?
 
Successful applicants will be invited to an initial telephone interview with one of our dedicated recruiters who will provide further details regarding this opportunity. 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
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 I

Salary

Location

US, Salisbury, NC

Location

Salisbury

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Research Site Services

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

JR117424

Expiry date

01/01/0001

Mitzi Overton

Author

Mitzi Overton
Read more Shortlist Save this role
CRA II or Senior CRA

Salary

Location

Canada, Burlington

Department

Clinical Monitoring

Location

Burlington

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Requirements: 12+ months of monitoring experience as a CRA for a sponsor or CROOncology experience as a CRA Located in Ontario, Canada At ICON, it’s our people that set us apart. Our diverse teams ena

Reference

JR117798

Expiry date

01/01/0001

Sarah Wood

Author

Sarah Wood
Sarah Wood

Author

Sarah Wood
Read more Shortlist Save this role
Study Start-Up Associate II

Salary

Location

Argentina

Department

Clinical Monitoring

Location

Argentina

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

The Study Start-Up Associate (SSUA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in

Reference

2024-108919

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Laboratory Technician I

Salary

Location

US, San Antonio, TX, IDS

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

San Antonio

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Laboratory

Job Type

Temporary Employee

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

JR113018

Expiry date

01/01/0001

Alexis Henry

Author

Alexis Henry
Read more Shortlist Save this role
Clinical Trial Coordinator

Salary

Location

Netherlands

Department

Clinical Monitoring

Location

Netherlands

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 organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-109724

Expiry date

01/01/0001

Vanessa Verdickt Read more Shortlist Save this role
Clinical Sample Processor

Salary

Location

US, Portland, OR

Department

Full Service - Development & Commercialisation Solutions

Location

Portland

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Supplies

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

JR118999

Expiry date

01/01/0001

Frank Lampart

Author

Frank Lampart
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above