Statistical Programmer

Integrated Resources Inc.; East Hanover (NJ); On-site; USD 75,000 - 95,000; Full time

Job summary

A leading company in the clinical research field is seeking a candidate with a strong background in data review and analysis using SAS. The role involves developing data review tools and ensuring the quality of reporting for oncology clinical trials, requiring proficiency in SDTM and knowledge of clinical trial processes.

Qualifications

• At least 2 years of work experience using SAS in data review and analysis.
• Knowledge of SDTM database design/structures.
• Experience in research programming preferred.

Responsibilities

• Develop standard global data review tools for oncology trials.
• Ensure quality and timelines of data review reporting deliverables.
• Participate in meetings covering data review reporting activities.

Skills

SAS

Data analysis

Communication

Tools

SDTM database

Jreview

Job description

Candidate to develop standard global data review tools, such as patient profiles, data quality checks, exception reports, PD reports, listings and figures for oncology trials.

Ensure timelines and adequate quality of data review reporting deliverables for assigned trials. Follow processes and adhere to Client and project specific standards as well as Health Authority requirements (SOP's, Master Analysis Plan, GCP and Regulatory Guidelines).

Comply with project/study programming standards and specifications following internal guidelines.

Provide input in Specifications, CRF and Data structure.

Participate as required at all meetings, discussions and activities covering aspects of data review reporting on trial level activates. Maintain efficient interfaces with internal and external customers.

Qualifications

At least 2 years of work experience using SAS in the data review, analysis and/or the reporting of pharmaceutical data. Working knowledge of SDTM database design/structures. Knowledge of other data review/statistics software packages like Jreview. SAS software systems experience. Experience in research programming preferred. Knowledge about clinical trials a plus. Ability to perform effectively in team environment and good communications skills required.