We are looking for a SAS Programmer to join our team!

The Associate Programmer will work closely with the Biostatistics, Data Management, Regulatory Operations & Statistical Programming groups to support the quality of clinical databases and contribute to the analysis and reporting of clinical trial data.

In this position you will develop and execute SAS programs in accordance with detailed specifications to support:

  • External programmatic clinical database checks.
  • Data trending reports to ensure quality of data management, risk-based monitoring, and core lab tasks.
  • Reporting and presentation of data and development of derived datasets to meet client needs.

Additional tasks may include:

  • Assist with validation of specifications that define program requirements used to generate edit checks, analysis datasets, tables, listings and figures.
  • Contribute to the validation of standardized programming and processes.
  • Maintain company standards in programs, datasets and directory structure.
  • Participate in the preparation/review of Data Management process control documents, including but not limited to Data Management Plans, External Clinical Database Edit Check Specifications, reconciliation plans, and Data Transfer Agreements.
  • Assist with validation of databases and software as needed.
  • Assist with the transfer of data to other individuals within CPC or to sponsors/vendors.

Here’s what you will need to bring to the table:

  • A minimum of 1 year experience programming in SAS (v9.2+), preferably in a Windows environment.
  • A minimum of 1 year experience working in the pharmaceutical or biotechnology industry or other regulated healthcare setting is preferred.
  • A Bachelor’s degree in science or related field is preferred.
  • Knowledge of Data Management practices of pharmaceutical product development highly desirable.
  • Good interpersonal communication skills, organizational skills and a great attention to detail.
  • Ability to work as a member of a team.
  • Ability to comprehend study documentation and archival processes.
  • Knowledge of and compliance with FDA, ICH-GCP/regional regulatory guidelines and Standard Operating Procedures

Note: Viable applicants will be required to demonstrate their computer skills as well as pass a background check.

This is not a remote position; you will work the majority of time in the office in a team environment.

Please include a short cover letter with answers to the following questions:

  • Why would you be a good candidate for this position?
  • How many years of experience using SAS do you have?
  • Any gaps in your employment history? Please explain.
  • What are your salary expectations?
  • Do you have experience in data management, the drug development industry or related field?
  • Are you authorized to work in the United States?
  • Do you now or will you in the future require sponsorship for employment visa status (e.g., H-1B visa status)?

CPC offers a comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)

An Equal Opportunity Employer
CPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, national origin, gender, gender identity, veteran status, marital status, sexual orientation, age, disability, genetic information or any other status protected by applicable federal, state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.

Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team.