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Senior Statistical Programmer

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Senior Statistical Programmer on a 12+ month contract, remote (California candidates). Requires 7+ years SAS programming experience in life sciences, expertise in CDISC standards, and background in cardiovascular medical device trials.
🌎 - Country
United States
💱 - Currency
$ USD
💰 - Day rate
Unknown
Unknown
🗓️ - Date discovered
April 1, 2025
🕒 - Project duration
More than 6 months
🏝️ - Location type
Remote
📄 - Contract type
Unknown
🔒 - Security clearance
Unknown
📍 - Location detailed
California, United States
🧠 - Skills detailed
#Programming #CDISC (Clinical Data Interchange Standards Consortium) #Data Manipulation #Compliance #Data Integrity #Data Analysis #SQL (Structured Query Language) #SAS #ADaM (Analysis Data Model) #Macros
Role description
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Title: SR. SAS PROGRAMMER

Duration: 12+ Month Contract

Remote: (California Candidates)

Looking for a Senior SAS Programmer to support multiple studies! If you have advanced SAS programming skills and CDISC expertise, this is a great opportunity to work on innovative cardiovascular projects.

Key Responsibilities:

Develop and maintain SAS programs for clinical trial data analysis and reporting.

Work with CDISC standards (SDTM/ADaM) to ensure regulatory compliance.

Utilize PROC SQL, SAS Macros, and other advanced SAS techniques for efficient data manipulation.

Collaborate with biostatisticians, data managers, and clinical teams to support study needs.

Ensure data integrity, quality control, and validation of outputs.

Must Haves::

7+ years of SAS programming experience in the life sciences industry.

Prior experience in medical device clinical trials.

Strong background in cardiovascular therapeutic studies.

Expertise in CDISC (SDTM/ADaM) standards and regulatory compliance.

Advanced knowledge of PROC SQL, SAS Macros, and statistical reporting.