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THE COMPANY

PHASTAR is a multiple award-winning global biometric Contract Research Organization (CRO). We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. With offices across the UK, US, Germany, Kenya, Australia, India, China and Japan, PHASTAR is the second largest specialized biometrics provider globally, and the largest in the UK.

Our unique approach to data analysis, “The PHASTAR Discipline”, has led us to build a reputation for outstanding quality. With this as our core focus, we’re looking for talented individuals who share our passion for quality and technical expertise to join our team. We have opportunities available in our Beijing, Shanghai and Wuhan offices. Positions can be either office-based, remote or a hybrid within these regions.

WHY PHASTAR

Accredited as an outstanding company to work for, PHASTAR is committed to employee engagement, workplace satisfaction and ensuring a healthy work-life balance. We offer flexible working, part-time hours, involvement in developing company-wide initiatives, structured training and development plans, and a truly supportive, fun and friendly environment.

What’s more, when you join our team, PHASTAR will plant a tree in your honour, as one of our Environmental, Social and Governance (ESG) initiatives. So, not only would you get your dream job, you’ll also be helping to save the planet!

Principal Statistical Programmer

in China
Permanent
Start date: As soon as possible
Role and responsibilities

As a principal statistical programmer, you will hold a combined project leadership and hands-on technical programming role. Working across a range of phases and therapeutics areas, you will lead assigned studies ensuring they are delivered to optimal quality, on time and on budget.

Key Responsibilities:

  • Responsibility for overall project delivery, including clinical trial reports and other regulatory submission deliverables
  • Project management responsibilities, including allocating staff, predicting and planning resources
  • Act as a study expert for multiple studies, with an ability to clarify details on analysis methods for the internal PHASTAR team
  • Manipulation of data to produce analysis datasets, including SDTM and ADaM datasets
  • Production and review of Tables, Figures and Listings (TFLs) according to statistical analysis plans
  • Advise on internal, client and CDISC data standards
  • Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR's internal procedures
  • Function as a programming expert across numerous studies
  • Maintain a positive and engaging client relationship with regards to statistical/programming issues
  • Report on study progress to the PHASTAR management team
Experience
  • BSc, MSc or PhD in mathematics, science or IT related discipline
  • Experience working within a clinical trials environment (CRO or pharma)
  • Substantial experience performing statistical analysis using SAS
  • CDISC (SDTM and ADaM) experience
  • Proven project leadership experience
  • Excellent written and verbal communication skills

APPLY NOW

With the world’s eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques.

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