Statistical Programmers I with SAS® experience (FSP), SERBIA or POLAND

Posted 15 Hours Ago
Be an Early Applicant
Hiring Remotely in Serbia
Remote
Junior
Pharmaceutical
The Role
As a Statistical Programmer I at Parexel, you will utilize SAS® programming techniques to analyze and report clinical study data, ensuring quality and regulatory compliance. You will participate in creating electronic submission packages and respond to regulatory agency questions, while also developing your statistical knowledge.
Summary Generated by Built In

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 Statistical Programmers I in Poland and Serbia with Hematology/Oncology experience. The role is dedicated to a single sponsor.

Picture Yourself At Parexel:

As a Statistical Programmer I you will support various SAS® programming activities related to the analysis and reporting of clinical study data; you will use programming techniques to produce analysis datasets, tables, figures and data listings ensuring first-time quality, traceability and regulatory compliance.
What You'll Do At Parexel:

  • Improve/develop your SAS® programming skills and broaden knowledge of clinical trial industry.

  • Participate in preparation of electronic submission packages according to the industry standards.

  • Support response to regulatory agency questions.

  • Prepare input to publications and conference materials.

  • Develop statistical knowledge using 4GL and different SAS® procedures.

Required skills and experience:

  • Knowledge and experience in SAS® software.

  • 1-2 years of industry experience (CRO/Pharma/Biotech) is required.

  • Experience in Hematology or/and Oncology is required.

  • Experience in 4GL language.

  • Understanding the principles of statistics.

  • Attention to detail with a focus on quality.

  • BSc degree in statistics, econometrics, mathematics, informatics or a related field.

A little about us:
 

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.

Highly qualified and dynamic team. Multinational working environment. Smooth induction and training program. We offer competitive financial packages, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.

Applicants must be authorized to work in Serbia/Poland. We are unable to sponsor or take over sponsorship of an employment Visa.

Top Skills

4Gl
SAS
The Company
HQ: Durham, North Carolina
20,524 Employees
On-site Workplace

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.
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sexual preference or orientation, nationality or political beliefs.
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We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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