(Senior) Manager, Clinical Programming

US$130000 - US$180000 per annum
  1. Permanent
  2. Programming
  3. United States
San Diego, USA
Posting date: 28 May 2024

Senior Manager for Clinical Programming - Permanent - California

Proclinical is seeking a dedicated and detail-oriented Clinical Trials SAS Programmer. This is a permanent role which is based fully on-site in Pasadena or San Diego, California.

Primary Responsibilities:

The successful candidate will be responsible for developing and executing edit checks and patient profile software for clinical trials, creating data listing programs and ensuring accurate data collection and reporting. This role also involves interfacing with CROs, performing quality audits and contributing to the development of departmental standards and processes.

Skills & Requirements:

  • Bachelor's degree in life sciences or a technical field.
  • Proficiency in SAS. For example in data presentation and output delivery systems as well as complex data manipulation.
  • Knowledge of implementing edit checks and patient profiles in active clinical trials.
  • Excellent verbal and written communication skills.
  • Familiarity with CDISC standards and derivation of SDTM and ADaM specifications are positives.
  • Experience in data management is an advantage.
  • Proficiency in R is preferred.
  • Experience working with CROs is preferred.

The Senior Manager for Clinical Programming's responsibilities will be:

  • Develop and execute edit checks and patient profile software for clinical trials.
  • Create and run data listing programs for various personnel.
  • Collaborate with data management to ensure accurate data collection and reporting.
  • Participate in study team meetings and support data management activities.
  • Deliver results on time for ad-hoc data programming requests.
  • Support statistical programming from raw data to ADaM for efficacy and safety evaluations.
  • Interface with CROs and perform quality audits on their outputs.
  • Contribute to the development and implementation of departmental standards, applications, processes, and training.
  • Develop or support the preparation of standard operating procedures.


  • $130,000 - $180,000 annually

If you are having difficulty in applying or if you have any questions, please contact Jennifer Iantosca at (+1) 215-660-3706 or j.iantosca@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.