Senior Clinical Data Coordinator I

Phastar; Almería; Remote; EUR 70,000 - 110,000; Full time

Job summary

Phastar is seeking a Senior/Principal Statistical Programmer for a fully remote role in sponsoring clinical programs. You will be responsible for independent programming leadership, SDTM/ADaM specifications, and ensuring data quality across studies.

You will develop SAS and R programs for datasets, listings, tables, and graphs, and coordinate with CROs to deliver high-quality results. This position requires extensive experience in clinical programming and a proactive, autonomous mindset.

Qualifications

• Experience as a senior statistical programmer in clinical trials or pharma settings.
• Proven ability to oversee CRO programmers and ensure data deliverables meet quality standards.
• Expertise with SAS and R for clinical data analysis and reporting.

Responsibilities

• Generate SDTM and ADaM specifications, datasets, reviewer’s guide and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and complex graphs with statistics.
• Deliver high-quality programming outputs, validate, and maintain SAS and/or R programs for clinical development.
• Oversee CROs to ensure timely, consistent data delivery across studies.

Skills

SAS

R

SDTM

ADaM

Define.xml

Clinical programming

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