Sr. Programming Analyst

Posted 07 December 2022
LocationSan Diego
Job type Permanent
DisciplineLife Sciences
Contact NameEthan Cohen

Job description

Position: Sr. Programming Analyst

Metric Search is excited to be partnered with an established global CDMO. We are currently working to find a Senior Programming Analyst that can contribute to this company’s goal of developing treatments that prevent illness and support healthier lifestyles.

Company Information

Our client is a global CDMO that offers a broad range of services to help biopharmaceutical companies world wide.

They have provided a broad range of services from early phase drug discovery to custom development to manufacturing.

They have also supported numerous preclinical and and clinical small and large molecules as well as commercial small and large molecules.

The Role

Our client is looking to hire a Sr. Programming Analyst to join their growing and highly collaborative team.

The Senior Data Architect will primarily be responsible for leading the design, development, implementation and continuous improvement of various analytics repositories for use in Business Intelligence applications.


  • Leading all the programming activities, including planning, organizing, delegating, coordinating, and managing programming activities, from start to finish by overseeing all development, validation, and production of programs for a set of studies or multiple clients
  • Providing technical solutions o a wide range of problems with high levels of complexity.
  • Maintain and develop departmental procedures and standards.
  • Recommending technical and process solutions that can be used to to increase efficiency of project work.


  • Minimum 6 years of experience in the pharma/biotech industry with a Bachelor’s degree or 4 years of experience with a Master’s degree.
  • Experience in leading the programming activities for submission required
  • Excellent skills in SAS programming for clinical studies
  • Excellent clinical trial knowledge is preferred
  • Working knowledge of other software such as S-plus and WinNonlin is preferred
  • Excellent knowledge of industry standards, such as ICH guidelines, CDISC data standards, and FDA guidelines.

How to apply

Email a copy of your resume to