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Contract Pharmaceutical Sas Programmer Jobs in Indiana

micro1 AI

Director of Biostatistics

Indianapolis, IN · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

Carmel, IN · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

South Bend, IN · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

Fishers, IN · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

Evansville, IN · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

Fort Wayne, IN · Remote

$60 - $100/hr

... experience in pharmaceutical, contract research, hospital, or academic medical contexts ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

MMS

Senior Biostatistician - Remote (US)

Zionsville, IN · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... Strong programming and logic skills (working knowledge of SAS) * Ability to apply drug development ...

BioTalent

PLC Programmer

Lebanon, IN · On-site

$65K - $88K/yr

Pharmaceutical / Biopharmaceutical Manufacturing Project: Large-scale capital project / new ... Contract 16 Month Location: On-site Lebanon, IN Role Summary The CODESYS PLC Programmer will be ...

SpectronRx

Pharmaceutical Manufacturer

Indianapolis, IN · On-site

$28 - $34/hr

Manufacturing Specialist COMPANY OVERVIEW SpectronRx is a growing Contract Development and ... An associate's degree in chemistry, biochemistry, chemical engineering, or a related field, along ...

PIVOT Workforce

Project Engineer

Indianapolis, IN

$80K - $90K/yr

Our client specializes in delivering high-quality construction solutions for the pharmaceutical ... Participate in the review and interpretation of project drawings, specifications, and contracts ...

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All JobsContract Pharmaceutical Sas Programmer JobsContract Pharmaceutical Sas Programmer Jobs in Indiana

Contract Pharmaceutical Sas Programmer information

What is a contract pharmaceutical SAS programmer?

A Contract Pharmaceutical SAS Programmer is a professional who works on a contract basis to manage and analyze clinical trial data using SAS (Statistical Analysis System) software for pharmaceutical companies. Their primary responsibilities include programming, validating, and generating statistical reports that support drug development and regulatory submissions. They collaborate with statisticians, data managers, and clinical teams to ensure data integrity and compliance with industry standards such as CDISC. Contract programmers may work independently or through staffing agencies, often on multiple projects for different clients.

What are the key skills and qualifications needed to thrive as a contract pharmaceutical SAS programmer?

To thrive as a Contract Pharmaceutical SAS Programmer, you need strong programming skills in SAS, knowledge of clinical trial data, and a background in statistics or life sciences, usually supported by a relevant degree. Familiarity with CDISC standards (SDTM, ADaM), clinical data management systems, and experience with regulatory submission processes are highly valued. Attention to detail, problem-solving ability, and effective communication with cross-functional teams distinguish top performers in this role. These skills ensure accurate data analysis, compliance with industry standards, and successful collaboration in delivering reliable results for clinical studies.

What are some common challenges faced by contract pharmaceutical SAS programmers when working with multiple clinical trial projects simultaneously?

Contract Pharmaceutical SAS Programmers often juggle several clinical trial projects at once, which can present challenges such as managing tight timelines, adapting to varying data standards, and coordinating with multiple study teams. Effective communication and strong organizational skills are essential to ensure data quality and timely delivery. Additionally, contractors must quickly familiarize themselves with each sponsor’s unique processes and regulatory requirements, making flexibility and adaptability key to success in this role.

What is the difference between Contract Pharmaceutical Sas Programmer vs Contract Clinical SAS Programmer?

AspectContract Pharmaceutical SAS ProgrammerContract Clinical SAS Programmer
CertificationsTypically requires SAS certifications, pharmaceutical industry knowledgeRequires SAS certifications, clinical trial experience
Work EnvironmentPharmaceutical companies, biotech firms, CROs in drug developmentClinical research organizations, hospitals, CROs in clinical trials
Employer & Industry UsagePrimarily in pharmaceutical and biotech sectorsPrimarily in clinical research and trial management

Contract Pharmaceutical SAS Programmers focus on data analysis and reporting within pharmaceutical companies, while Contract Clinical SAS Programmers work mainly on clinical trial data across various research organizations. Both roles require SAS expertise and industry-specific knowledge, but their primary focus and work environment differ slightly.

Are Contract Pharmaceutical SAS programmers in demand?

Contract Pharmaceutical SAS programmers are in steady demand due to the ongoing need for data analysis and reporting in the pharmaceutical industry. Skills in SAS programming, clinical trial data management, and regulatory compliance increase employability, especially for contract roles that offer flexibility and specialized expertise.

How much do contract pharmaceutical SAS programmers make?

Contract pharmaceutical SAS programmers typically earn between $50 and $100 per hour, depending on experience, location, and project complexity. Senior programmers with specialized skills or certifications can command higher rates, especially for short-term or high-demand projects.

What are the most commonly searched types of Pharmaceutical Sas Programmer jobs in Indiana?

The most popular types of Pharmaceutical Sas Programmer jobs in Indiana are:

What cities in Indiana are hiring for Contract Pharmaceutical Sas Programmer jobs?

Cities in Indiana with the most Contract Pharmaceutical Sas Programmer job openings:

Contract Pharmaceutical Sas Programmer jobs near you

SR. CLINICAL SAS PROGRAMMER at cGxPServe Indianapolis, IN

Downtown Boulder Partnership

Indianapolis, IN • On-site

$100 - $130/hr

Other

Posted 17 days ago

Job description

Responsibilities
  • Perform data manipulation, analysis, and reporting of clinical trial data.
  • Develop and maintain department/system-level macros.
  • Create and review SDTM and Adam specifications.
  • Create and validate SDTM data sets.
  • Create and validate analysis data sets.
  • Create and validate patient profiles.
  • Program and generate tables, figures, and listings (TFLs).
  • Validate and document SAS programs and outputs.
  • Fulfil ad-hoc analysis requests.
  • Provide other services.
Requirements
  • Bachelor's degree or higher, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or a related applicable field.
  • Minimum of ten (10) years' SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
  • Ability to create source and validation programs using SAS software for SDTM datasets, Adam datasets, and tables, figures, and listings (TFLs) for multiple studies/products.
  • Experience integrating data across multiple studies or drug programs.
  • Expertise in developing and using system-level macro programs.
  • Experience programming with SAS/GTL.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
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