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Senior SAS / Statistical / Clinical Programmer

Company: N/A

Location: Nationwide, CA, USA, CA

Pay: N/A

Contact Information


Name: Ju Zhang
Phone: 877.267.1259
Fax: n/a
Apply Online

Job Description

TechData is hiring SAS Clinical Programmer, Statistical programmer (some telecommuting) and Biostatistician (some telecommuting), AX/MRP Specialist, Sr. Drug Safety Associate, Sr. Technical Editor for our pharmaceutical clients in Bay Area, CA. We also have similar positions in MA, PA, NJ, MD, and other parts of CA. Please see the requirements below and send your resume to: john.zhang@techdataservice.com or [Click Here to Email Your Resumé]. TechData is a leading provider for temporary and permanent positions in the pharmaceutical industry. TechData offers the most competitive pay rates and benefits in clinical research consulting services.





Sr. Statistical/SAS Programmer (some positions can be telecommuting)


Work Experience:




Management of Staff:



Functional/Technical Knowledge & Skills (including any required proficiency for particular computer programs or applications, if applicable):




Customer & Industry Knowledge:



 


Required Skills:


 



Education:


Must have a science degree and 2+ years working in a pharmaceutical/research environment. Advanced degree in Science or Mathematics preferred. 


 

Sr. SAS Clinical Programmer


The role is accountable for the arrangements and timely delivery of all Clinical Programming (CP) aspects of assigned trials.




  1. Review routine specifications drafted by support programmers or study team members, revise if needed with input from team

  2. Gather requirements from study team and write complex specifications for metrics or reports for assigned studies

  3. Ensure end users have sufficient detail (QC listings, support data presentation) in addition to the formal deliverables to evaluate them for approval

  4. Maintain change logs as specifications are revised or updated

  5. Provide support in development and implementation of improved clinical programming processes, SOPs, methods, and deliverables. Identifies areas of deficiency requiring new or updated SOPs or guidelines

  6. Provide support in the development of standard deliverables, specifications, and programming




  1. Send reviewed/completed specifications for programming

  2. Answer technical questions from programmers, or coordinate with end users for  clarifications if needed

  3. Ensure support programmers (in-house or CRO) meet timelines, or escalate any at risk

  4. Review programmed output against the specifications

  5. Coordinate end user review and address any feedback

  6. Release finalized programming into production





Work Experience and Educational Requirements:


Bachelor’s in Computer Sciences, Mathematics or Life Sciences with a minimum of 5 – 8 yrs. of clinical or statistical programming experience in the pharmaceutical or biotechnology industry, or MA/MS with 4 yrs. of experience.












Job Requirements

Sr. Statistical/SAS Programmer (some positions can be telecommuting)


Work Experience:




Management of Staff:



Functional/Technical Knowledge & Skills (including any required proficiency for particular computer programs or applications, if applicable):




Customer & Industry Knowledge:



 


Required Skills:


 



Education:


Must have a science degree and 2+ years working in a pharmaceutical/research environment. Advanced degree in Science or Mathematics preferred.