Senior Clinical Data Coordinator I

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

Job summary

Phastar is seeking a Senior/Principal Statistical Programmer with SAS + R expertise to join a sponsor-dedicated, remote role. You will work on clinical development programs, oversee CROs, and deliver high-quality data outputs for regulatory submissions.

The role requires independent programming, SDTM/ADaM knowledge, and ability to produce complex tables, listings, and graphs. Collaboration with statisticians and sponsors is essential, with emphasis on data integrity and timely delivery.

Qualifications

• Experience in clinical development settings.
• Proficiency in SAS and R for production of listings and graphs.
• Strong communication and collaboration with CROs and sponsors.

Responsibilities

• Develop SDTM/ADaM datasets and define.xmls for studies.
• Create complex tables, listings, and graphs using SAS and R.
• Support CROs and ensure timely, high-quality deliverables.

Skills

Statistical programming

Independent work

Tools

SAS

R

SDTM/ADaM

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