Senior Programmer - Remote Canada (Internal Project) Job at PHASTAR
Overview:
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, 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! Responsibilities:
Key Responsibilities:
ABOUT PHASTAR
PHASTAR is a multiple award-winning global biometrics 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. Operating across the UK, US, Canada, France, Spain, Germany, Kenya, Australia, India, China, and Japan, PHASTAR is the second largest specialized biometrics provider globally, and the largest in the UK.
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, 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!
As a Senior Statistical Programmer, you will hold a combined project leadership and technical hands-on programming role. Working on a range of phases and therapeutic areas, you will lead assigned studies, ensuring they are delivered to optimal quality, on time and on budget.
Key Responsibilities:
Project leadership of assigned studies- 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
- Creation and review of programming specifications and, if required, annotation of case report forms (CRFs) to CDISC standards
- Feeding back data errors to client data management teams
- Attendance at regular client meetings to provide updates on projects and timelines
- Working to industry (CDISC) and client standards
- BSc, MSc or PhD in Mathematics, Science or IT related disciplineExperience working within a clinical trials environment (CRO, pharma or clinical trials unit)
- Substantial SAS programming experience
- Previous experience working on oncology clinical trials (advantageous not essential)
- CDISC (SDTM and ADaM) experience
- Previous project leadership experience
- Excellent written and verbal communication skills
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