Senior Storyboard Concept Artist (Games | Visual Storytelling)

Jobgether; Málaga; Remote; EUR 70,000 - 90,000; Full time

Job summary

Jobgether is recruiting a Senior/Principal Statistical Programmer SAS + R (Remote) to be sponsor-dedicated, embedded with one of our pharmaceutical clients, with Cytel support behind you through every step of the project.

You will act independently with minimal supervision, lead data analysis and reporting activities for clinical trials, and oversee CRO programmers to ensure consistent, high-quality outputs. The role offers autonomy, exposure to multiple therapeutic areas, and a dynamic team.

Responsibilities

• Independent work with minimal supervision and tracks progress.
• Oversees CRO programmers to ensure consistent, high-quality data summaries.
• Implements all reporting and analysis activities for sponsor clinical trials.

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.