Senior Statistical Programmer for Study Data & Submissions

Scorpion Therapeutics; New Jersey; On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics in New Jersey is seeking a programmer to support or lead programming and quality control of analysis datasets, tables, listings and graphs for clinical studies.

You will coordinate activities and communicate shifting timelines to the study team, create and maintain programming specifications for analysis datasets, and support submission requirements including annotated CRFs and define documents.

Qualifications

• Master’s degree with 3+ years of relevant experience.
• Proven programming experience supporting clinical study data and analysis deliverables.
• Strong documentation and quality control skills within a regulated environment.
• Experience collaborating within a multidisciplinary study team.

Responsibilities

• Support or lead programming and quality control of analysis datasets, tables, listings, and graphs
• Coordinate activities and communicate shifting timelines and milestones to the study team
• Create and maintain programming specifications for analysis datasets across studies
• Support creation and validation of submission requirements (including annotated CRFs and define documents)
• Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch
• Provide programming support for presentations and statistical ad hoc requests
• Participate in department working groups; contribute to tool development and process improvement
• Design and test program logic independently; maintain documentation in a regulated environment

Skills

Programming experience

Documentation and quality control

Cross-disciplinary collaboration

Analytical thinking

Maintaining code quality

Education

Master’s degree

Job description

Scorpion Therapeutics in New Jersey is seeking a programmer to support or lead programming and quality control of analysis datasets, tables, listings and graphs for clinical studies.

You will coordinate activities and communicate shifting timelines to the study team, create and maintain programming specifications for analysis datasets, and support submission requirements including annotated CRFs and define documents.