Senior Statistical Programmer

JOB OVERVIEW

Description

The Statistical Programmer Provides support to the lead programmer and the study team on all programming activities according to the study requirements and the timelines. This role contributes to studies in various therapeutic areas and all clinical trial phases. The incumbent implements and executes the programming and project standard under general supervision of the lead programmer and manager to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. Maintains programming documentations such as study tracker, code, logs, and analysis outputs in a regulated environment. The incumbent may participate in and contribute to department goals and SME topics.

Major Duties And Responsibilities

• Provide programming support within multiple studies/projects in various study activities with timely and high-quality programming deliverables in assigned tasks and projects
• Work with lead programmer and manager in cross-functional collaborations to support the study conduct and reporting activities.
• Maintain all documentation in accordance with SOPs/Guidance/WI/process to ensure traceability and regulatory compliance
• Participate and contribute towards department goals and SME topics

Secondary Duties And Responsibilities

• Adhere to Regeneron processes and policies around retention of data, records, and information for clinical trials.
• Show commitment to and perform consistently to ensure high quality deliverables.

Education

• MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.
• SAS Certification a plus.

Skillset/Essential Requirements

• Proficiency in SAS. Knowledge of other programming languages such as R, Python etc. is a plus.
  • SAS, (Base, Stat, Macro, graph)
• Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles) is a plus
• Ability to work on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Positive attitude, team player and growth mindset

COMPANY DESCRIPTION

A world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations

Tagged as: Python, R, SAS