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Form of workABOUT PHASTAR
PHASTAR is a specialist biometrics contract research organization offering statistical consulting, clinical trial reporting, data management, and data science services.
With offices across the UK, US, Germany, Denmark, 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.
WHY PHASTAR
A career at PHASTAR offers you the chance to work in an intellectually stimulating, dynamic and supportive environment, where you will play an important role in the development of the next generation of lifesaving medicines.
Our ever-growing customer base provides access to work in many areas of interest and, as PHASTAR strongly believes in investing in employees’ growth and development, we offer a wide range of training opportunities across all levels.
We offer flexible working, a healthy work-life balance, involvement in developing company-wide initiatives, and a fun and friendly working environment that is renowned within the industry!
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.
Demand for our Functional Service Provision is continuing to grow, and we’re looking for an experienced Statistical Programmer to join our team in the US (remote).
As a statistical/senior programmer working within FSP, you will be fully integrated into our sponsor’s neuroscience team as a key contributor, providing that partner with hands-on technical programming support.
Key Responsibilities:
- Create and QC SDTM and ADaM specifications
- Produce and review Tables, Figures and Listings (TFLs) according to statistical analysis plans
- May be involved in complex ADaM programming
- Annotate aCRF
- Create and review P21 reports
- Work independently and communicate effectively with the client
- BSc, MSc or PhD in mathematics, science, or IT related discipline
- Experience working on clinical trials within a CRO/pharmaceutical environment
- Advanced SAS programming skills with the ability to perform end-to-end programming tasks
- Substantial CDISC SDTM and ADaM experience with the ability to perform complex ADaM programming
- Experience running P21 report, identifying issues, and implementing updates
- SAS macro experience
- Define/ADRGs/SDRGs experience advantageous but not essential
- Excellent written and verbal communication skills with the ability to work independently
- Previous experience working on neuroscience clinical trials advantageous but not essential
APPLY NOW
Our FSP positions provide the unique opportunity to work for an award-winning CRO that is recognized for its continuous learning and development opportunities, technical expertise, outstanding quality, and cutting-edge data science techniques, whilst also gaining direct experience of working within our sponsor’s pharmaceutical environment. Apply now to submit your application.
