Senior Clinical Data Coordinator I

Phastar; Barcelona; Remote; EUR 55,000 - 90,000; Full time

Job summary

Phastar is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely with sponsor-dedicated support from Cytel. You will be responsible for implementing reporting and analysis activities for clinical trials across multiple studies and therapeutic areas.

The role involves generating SDTM/ADaM specifications, creating datasets, listings, tables, and figures, and overseeing CRO programmers to maintain high-quality data delivery.

Qualifications

• Clinical development experience preferred.
• Experience delivering SDTM/ADaM outputs.

Responsibilities

• Generate SDTM, ADaM specs, datasets, reviewer's guide and define.xml for multiple studies.
• Develop SAS programs to generate datasets, complex listings, tables and graphs.
• Deliver high-quality statistical programming results using SAS and/or R.
• Oversee CROs to ensure timely and accurate data delivery.

Education

Bachelor's degree in Statistics/Biostatistics

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