Senior Statistical Programmer - FSP - ( Permenant,homebased/remote) Evergreen

IQVIA; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a Senior Statistical Programmer to join their dynamic Global Biostatistics team. In this role, you will leverage cutting-edge technology to develop programming solutions that meet the needs of internal and external clients. With a strong focus on career development, you will have the opportunity to work on global projects across various therapeutic areas while collaborating with a supportive team. This role is perfect for someone passionate about data and its impact on healthcare, providing a chance to make a significant difference in patients' lives through innovative solutions and insights.

Benefits

Global exposure

Collaborative team environment

Access to innovative technology

Excellent career development opportunities

Work-Life Balance

Qualifications

• 5+ years of Statistical Programming experience in Life-Science.
• Strong understanding of clinical trial data and data manipulation.

Responsibilities

• Develop integrated programming solutions for statistical needs.
• Lead studies and coordinate tasks within programming teams.

Skills

Statistical Programming

SAS Base

SAS Graph

SAS Macros

CDISC standards (SDTM and ADaM)

Data Manipulation

Client Engagement

Project Coordination

Education

Bachelor's in Computer Science

Master's in Mathematics

Tools

SAS

Statistical Software

Job description

Senior Statistical Programmer - FSP - (Permanent, homebased/remote) Evergreen

Pay Competitive

Location: London/England

Employment type: Full-Time

Job Description

• Req#: R1409379

Senior Statistical Programmer

Global Biostatistics

Home-based, office-based, hybrid options available

Join us on our exciting journey!

The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA is experienced in submissions for all major regions; working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.

IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.

Job Overview:

As a Senior Statistical Programmer, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.

Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.

You will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients’ needs.

You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. You will also estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.

Requirements:

• Bachelors or Masters in Computer Science, Mathematics or equivalent
• 5+ years Statistical Programming experience within the Life-Science industry
• Experience in SAS Base, and good knowledge of SAS graph and SAS Macros
• Excellent knowledge of CDISC standards (SDTM and ADaM)
• Excellent application development skills
• Strong understanding of clinical trial data and extremely hands-on in data manipulations, analysis, and reporting of analysis results.
• Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Join IQVIA to see where your skills can take you

• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on positive well-being

Unleash your potential!

It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.

When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

About the company

IMS Health and Quintiles are now IQVIA. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, technology, and data.