About the role
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel is currently seeking a Statistical Programmer II to join us in either Serbia or Poland, dedicated to a single sponsor.
This role will provide technical expertise for the conduct of clinical trials and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part of that role) on small, non-complex projects.
Working as a Statistical Programmer II at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Responsibilities
Deliver best value and high-quality service working on client system and following client processes.
Work closely with client teams and Parexel colleagues in global environment.
Specialize in one of the following therapeutic area: hematology/oncology/cell therapy.
Use SAS programming to produce derived datasets (ADaM), tables, figures, and data listings of varying complexity.
Develop and QC derived dataset specifications and other process supporting documents.
Ensure all work maintains complete traceability and regulatory compliance.
Participate and contribute to knowledge-sharing sessions with programming community.
Here are a few requirements specific to this advertised role.
Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences.
Minimum 3 years of SAS programming experience in clinical research.
Proficiency in SAS Base, SAS/STAT, SAS/GRAPH, and SAS macros.
Strong understanding of CDISC standards.
Knowledge of statistical terminology, clinical tests, and protocol designs.
Excellent attention to detail with a focus on quality.
Strong written and verbal English communication skills.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
Parexel has a fully flexible work arrangement - you can be fully home based. But if you live close to our office and you want to use it, you are always welcome, and we will keep the desk ready for you!
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Originally posted on Himalayas