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Intern Remote Sas Programmer Jobs in Massachusetts

... SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values * We believe ...

Performs quality control checks of SAS code and output produced by other Statistical Programmers to ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

Each AI Native Intern is embedded in a real team, working on real problems, and is expected to ... engineers to focus on higher-order problems. This is a fully remote position. The program runs ...

Each AI Native Intern is embedded in a real team, working on real problems, and is expected to ... engineers to focus on higher-order problems. This is a fully remote position. The program runs ...

$15.25 - $20.25/hr

Our data security posture management platform is engineered specifically to address modern data ... Remote Duration: 10-12 weeks (Summer 2025)

$15 - $19.75/hr

Our data security posture management platform is engineered specifically to address modern data ... Remote Duration: 10-12 weeks (Summer 2025)

Sr Manager, Statistical Programming

Boston, MA · On-site +1

$151K - $172K/yr

Proficient in SAS * Good knowledge of CDISC ADaM and SDTM * Strong knowledge of relevant regulatory ... On-site in Boston (recommended 2-3 days hybrid) or 100% remote with occasional travel to Boston ...

New

Program Manager

Boston, MA · Remote

$90K - $130K/yr

San Francisco, CA or Boston, MA (Semi-remote organization with hubs in both cities) Role Overview ... engineering, IT). * Experience with a statistical software package (e.g., Stata, SAS, SPSS, R)

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Intern Remote Sas Programmer information

What is the difference between Intern Remote Sas Programmer vs Intern Remote Data Analyst?

AspectIntern Remote Sas ProgrammerIntern Remote Data Analyst
Required CredentialsBasic programming knowledge, SAS certification (preferred)Statistical or data analysis coursework, basic programming skills
Work EnvironmentRemote, team-based projects in healthcare, finance, or researchRemote, data-focused tasks across various industries
Employer & Industry UsageUsed in industries relying on SAS for data managementUsed across industries for data interpretation and reporting
Search & Comparison IntentUnderstanding roles involving SAS programming at entry levelComparing entry-level data analysis roles

The Intern Remote Sas Programmer typically focuses on developing SAS scripts for data management and analysis, requiring basic SAS knowledge and certifications. In contrast, the Intern Remote Data Analyst handles broader data interpretation tasks, often using multiple tools. Both roles are remote and industry-specific but differ in technical focus and skill requirements.

What are the most commonly searched types of Remote Sas Programmer jobs in Massachusetts? The most popular types of Remote Sas Programmer jobs in Massachusetts are:
What cities in Massachusetts are hiring for Intern Remote Sas Programmer jobs? Cities in Massachusetts with the most Intern Remote Sas Programmer job openings:

Senior Statistical Programmer FSP

Cytel

Cambridge, MA • On-site, Remote

Full-time

Posted 20 days ago


Job description


Sponsor-dedicated:
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview:
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our values
  • We believe in applying scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
  • We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities
How you will contribute:
  • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
  • Production and QC / validation programming
  • Generating complex ad-hoc reports utilizing raw data
  • Applying strong understanding/experience of Efficacy analysis
  • Creating and reviewing submission documents and eCRTs
  • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
  • Performing lead duties when called upon
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change

Qualifications
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
  • Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
  • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a master's degree or above.
  • Study lead experience, preferably juggling multiple projects simultaneously preferred.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Strong QC / validation skills.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.
  • Experience supporting immunology, respiratory or oncology studies would be a plus.
  • Excellent analytical & troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.