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

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 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 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. As well as,
estimating 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 a 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. #J-18808-Ljbffr