SAS Data Programmer

2 weeks ago

Uxbridge Greater London, United Kingdom Bristol-Myers Squibb Full time
Senior Statistical Programmer page is loaded Senior Statistical Programmer
Apply locations Uxbridge - GB time type Full time posted on Posted 6 Days Ago job requisition id R Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity.

Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.

We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.


Read more:

Position Summary

Provide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of Bristol Myers Squibb (BMS) products.

This position is primarily responsible for the design, development and implementation of technical solutions for integrating, analyzing and reporting clinical data.

Senior Statistical Programmers develop collaborative relationships and work effectively within Global Biometrics & Data Sciences (GBDS), with external vendors and members of cross-functional development teams.

Direct Reports
None. Possible contractors/leased workers.
Vendor Oversight
Yes
Key Business Partners
Internal/external stakeholders, project team members, vendors
Key Responsibilities
Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs
Provides programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis
Support the electronic submission preparation and review
Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities
Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors
Independently leads and / or performs programming assignments with minimal supervision
Support improvement initiatives
Skills, knowledge, and experience

Minimum Requirements:
~ Bachelor's degree in statistics, biostatistics, mathematics, computer science or life sciences required.
~5 years programming experience in industry recommended.
~ Demonstrated proficiency in using SAS, R or other programming languages to produce derived analysis datasets and TFLs.
~ Have in-depth understanding of clinical data structure (e.g. CDISC standards) and relational database.
~ Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21.
~ Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.
~ Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.
~ Have good understanding of regulatory, industry, and technology standards and requirements.
~ Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs.
~ Demonstrated ability to work in a team environment with clinical team members.

Preferred Requirements:
Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)
Oncology experience
Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements
Experience in other software packages (e.g. R)
Experience with the Linux operating system
#LI-Hybrid

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway.

You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary.

Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs.

The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility.

For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture.

For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.

Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.

If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to .

Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities.

As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb is Disability Confident – Committed
A UK Government scheme
W e're creatinginnovative medicines for patients fighting serious diseases. We're also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
#J-18808-Ljbffr

  • SAS Data Programmer

    2 weeks ago

    Uxbridge, Greater London, United Kingdom Regeneron Pharmaceuticals, Inc Full time

    The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal...

  • SAS Data Programmer

    2 weeks ago

    London, Greater London, United Kingdom Lifelancer Ltd Full time

    As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. How you will contribute:Performing data manipulation, analysis and reporting of clinical trial data, both safety and...

  • SAS Data Programmer

    2 weeks ago

    London, Greater London, United Kingdom Healthcare Businesswomen's Association Full time

    About the role 100,000+ That's how many patients participate in our clinical trials at any given time. GCO is Novartis' powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and...

  • SAS Data Programmer

    2 weeks ago

    London, Greater London, United Kingdom Warman O'Brien Full time

    Senior Statistical Programmer | Pharma | Fully Home Based | UK | Warman O'Brien are working with a Global Pharma who due to continued success and growth in the UK, have several opportunities for experienced Senior Statistical Programmers to join them. As a Senior Statistical Programmer, you will have an advanced knowledge of Statistical Programming and data...

  • Contract SAS Programmer

    3 months ago

    London, United Kingdom Medpace Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Contract SAS Programmer

    1 month ago

    London, United Kingdom Medpace Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Contract SAS Programmer

    4 weeks ago

    London, United Kingdom Medpace Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Contract SAS Programmer

    4 weeks ago

    London, United Kingdom Medpace Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Sas Analyst

    4 weeks ago

    London, United Kingdom Harnham - Data & Analytics Recruitment Full time

    **SAS Analyst** **£300 -£400 PER DAY- OUTSIDE IR35** **3 MONTHS LONDON HYBRID** Are you confident in managing large amounts of data using SAS and Google sheets? A global retail company is looking for an experienced SAS analyst to come in and assist manage the flow of their data. **THE COMPANY** This company is one of the biggest and most recognizable...

  • Sas Analyst

    4 weeks ago

    London, United Kingdom Harnham - Data & Analytics Recruitment Full time

    **SAS Analyst** **£300 -£400 PER DAY- OUTSIDE IR35** **3 MONTHS LONDON HYBRID** Are you confident in managing large amounts of data using SAS and Google sheets? A global retail company is looking for an experienced SAS analyst to come in and assist manage the flow of their data. **THE COMPANY** This company is one of the biggest and most recognizable...

  • Contract SAS Programmer

    3 months ago

    London, United Kingdom Medpace, Inc. Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Contract SAS Programmer

    1 month ago

    London, United Kingdom Medpace, Inc. Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Contract SAS Programmer

    4 weeks ago

    London, United Kingdom Medpace, Inc. Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • Contract SAS Programmer

    4 weeks ago

    London, United Kingdom Medpace, Inc. Full time

    Due to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an...

  • SAS Data Programmer

    2 weeks ago

    London, Greater London, United Kingdom AIXIAL GROUP Full time

    The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Czech Republic, Switzerland, Denmark, Romania, and India. The CRO occupies a unique position in the clinical...

  • SAS Data Programmer

    2 weeks ago

    London, Greater London, United Kingdom Proclinical Staffing Full time

    This role is an instrumental part in running and overseeing programming at the study and program level as well as ensuring all work is of the highest quality standards. Implement effective resource planning, task allocation, and tracking of workload in accordance with agreed metrics and quality standards. Supply highquality programming that consistently...

  • Senior SAS Programmer

    2 weeks ago

    London, Greater London, United Kingdom IQVIA Argentina Full time

    Senior Statistical Programmer Home-based, office-based, hybrid options available The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are 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...

  • Senior SAS Programmer

    2 weeks ago

    City of London, Greater London, United Kingdom Proclinical Staffing Full time

    Job Description Proclinical is seeking a dedicated Principal Statistical Programmer to become part of a global Biostatistics and Programming team. This role is an instrumental part in running and overseeing programming at the study and program level as well as ensuring all work is of the highest quality standards. Implement effective resource planning, task...

  • Senior SAS Programmer

    3 weeks ago

    London, United Kingdom CK GROUP Full time

    CK Group is recruiting for a Senior SAS Programmer, to join a leading Pharmaceutical company who have an excellent reputation and are based in London. **Senior SAS Programmer Role**: - Responsible and accountable for all programming aspects of a clinical study and where appropriate the development project(s). - Being the primary OPUK contact for all...

  • Senior SAS Programmer

    1 month ago

    London, United Kingdom IQVIA Argentina Full time

    Senior Statistical Programmer Home-based, office-based, hybrid options available The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are 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...