Senior Clinical Data Coordinator I

Phastar; Córdoba; Remote; EUR 65,000 - 90,000; Full time

Job summary

Phastar is seeking a Senior/Principal Statistical Programmer (Remote) to join a sponsor-dedicated program. You will work within one of our pharmaceutical clients, delivering high-quality SDTM/ADaM specifications and supporting data delivery with SAS and R.

You’ll oversee CRO programmers and contribute to multiple studies with autonomy. You will report to the Biostatistics and Programming leadership and play a key role in producing datasets, listings, tables, graphs and define.xmls across

Qualifications

• Generate SDTM and ADaM specifications and define.xml for studies.
• Develop SAS programs to create datasets, listings, tables and graphs.
• Deliver high-quality programming results and maintain SAS/R programs.
• Oversee CROs to ensure data delivery quality.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer’s guide and define.xml.
• Develop SAS programs to create datasets, listings, tables and graphs.
• Deliver high-quality statistical programming results and maintain SAS and/or R programs.
• Participate in overseeing CROs.

Skills

SAS programming

R programming

Clinical data programming

CRO oversight

Tools

SAS

R

Job description

Senior/Principal Statistical Programmer SAS + R (Remote)

Sponsor-dedicated:
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview:
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
As a Principal Statistical Programmer, your responsibilities will include:

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
• Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
• Participate in overseeing CRO's