Regarding this position:
Join us in working your magic!
Are you prepared to investigate, dismantle obstacles, and learn more?  Like you, we are aware of your ambitious aspirations!  Our colleagues across the world are passionate about using science and technology to improve people's lives via our solutions in electronics, healthcare, and life science.  We have huge dreams together and are committed to taking care of our diverse population, clients, patients, and the environment.  For this reason, we are constantly searching for inquisitive brains that share our ability to imagine the unthinkable.
Our goal as United As One for Patients is to contribute to the creation, enhancement, and extension of life.  In therapeutic domains including oncology, neurology, and fertility, we create medications, smart gadgets, and cutting-edge technology. In order to assist patients at every stage of life, our teams collaborate passionately and with unwavering curiosity across six continents.  Joining our healthcare team offers fantastic chances for professional progression and personal growth worldwide, as well as a varied, inclusive, and flexible work environment.
Your part:
Working with cutting-edge technological solutions like R, Shiny, and SAS will provide you the chance to manage asset teams and successfully train junior employees as a Senior Principal Statistical Programmer.  You will influence strategic choices in statistical programming while contributing to global assets in a range of therapeutic domains.
As the Lead Statistical Programmer, your duties will involve overseeing the trial or asset programming team and making sure that the delivery of trials and assets complies with quality standards and deadlines.  You will produce SDTM and ADaM datasets and create specifications, among other programming tasks, at both the trial and asset levels. You will also construct datasets for integrated analyses such as ISS or ISE and produce and validate analytical outputs in compliance with the Statistical Analysis Plan.  Additionally, you will be in charge of carrying out ad hoc programming tasks in response to requests from both internal and external sources.  By actively participating in statistical programming projects, you will encourage process enhancements and creativity while offering trial and asset teams professional counsel, direction, and training, so promoting the skill development of your colleagues.
Who are you?
. BSc or MSc (in a numerical field, ideally computer science, statistics, or mathematics)
in least nine years of directly relevant experience is required, as well as shown performance in a statistical programming capacity in clinical development in a pharmaceutical or biotech company or at a CRO.  Experience working in a global setting is advantageous.
Proficiency with R and SAS
complete knowledge of the underlying ideas and specifications of the CDISC SDTM and ADaM standards, including the reviewers' guide, Define.xml, and specifications.
Strong grasp of procedures relevant to clinical development programs, Experience in directing e-submission processes is advantageous.
Proven capacity to efficiently manage resources, guaranteeing prompt delivery and high-quality results
the capacity to offer answers to challenging programming problems and assess potential solutions to choose the best ones.
What we have to offer: 
We are inquisitive individuals with a diverse range of experiences, viewpoints, and backgrounds.  We embrace variety in all its forms and think it fosters creativity and quality, enhancing our capacity to lead in science and technology.  Our goal is to make it possible for everyone to learn and change at their own speed.  Come help us create a culture of belonging and inclusion that affects millions of people and gives everyone the confidence to do their best job and advance humanity!