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Entry Level Remote Base Sas Programmer Jobs in Waterbury, CT

KEYENCE

Field Application Engineer '27

Rocky Hill, CT · On-site +1

$53K - $80K/yr

Provide on-call, on-site and remote technical support, training, and troubleshooting * Travel ... Base Salary: $53,940 - $80,760 (based on location) * Performance Bonus Target: $24,000 annually ...

Ameresco

DER Monitoring Platform Technician

Waterbury, CT · On-site +1

$25.48 - $37/hr

Ameresco has an immediate opening for a DER Technician this is an entrylevel, position responsible ... Associate or bachelor's degree in a STEM field (e.g., Engineering Technology, Electrical ...

PaceMate

Loop Recorder Device Specialist

West Haven, CT · On-site +1

$34.61 - $44.23/hr

Loop Recorder Device Specialist Location: 100% Remote (U.S. - candidates must reside in the ... Integrate a knowledge base from physiology, pathophysiology, and cardiac device function to perform ...

All JobsBase Sas Programmer JobsEntry Level Remote Base Sas Programmer JobsEntry Level Remote Base Sas Programmer Jobs in Waterbury, CT

Entry Level Remote Base Sas Programmer information

See Waterbury, CT salary details

$14

$50

$81

How much do entry level remote base sas programmer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for entry level remote base sas programmer in Waterbury, CT is $50.08, according to ZipRecruiter salary data. Most workers in this role earn between $35.14 and $62.88 per hour, depending on experience, location, and employer.

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Entry Level Remote Base Sas Programmer jobs near you
Infographic showing various Entry Level Remote Base Sas Programmer job openings in Waterbury, CT as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $104,165 per year, or $50.1 per hour.

Manager, Clinical Programming (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Re-posted 8 days ago

Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by delivering high-quality programming solutions for medical monitoring, data management, and statistical programming activities. The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern programming tools including SAS and R. This role partners closely with cross-functional teams to develop efficient, compliant, and scalable programming solutions that support ongoing clinical trials

Key Responsibilities Provide programming support for medical monitoring, data management, and statistical programming activities across clinical studies. Develop specifications for SDTM dataset creation in accordance with CDISC SDTM Implementation Guide (SDTM IG). Program, validate, and maintain CDISC-compliant SDTM datasets.

Create and maintain annotated CRFs (aCRFs) aligned with SDTM specifications. Generate outputs and listings to support medical monitoring, data review, statistical endpoint monitoring, and data management activities. Develop, enhance, and maintain SAS macros, R functions, and other reusable programming utilities.

Design, develop, test, and implement programming solutions to address complex business and study requirements. Ensure programming deliverables meet quality standards, timelines, and regulatory expectations. Collaborate effectively with cross-functional teams including Biostatistics, Data Management, Clinical Operations, and Medical Monitoring.

Manage multiple projects simultaneously while delivering high-quality work within established timelines. Qualifications Bachelor's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline (or equivalent experience). Experience programming in the pharmaceutical, biotechnology, or related regulated industry preferred.

Advanced programming proficiency in SAS, R, and SQL. Strong working knowledge of CDISC standards, including SDTM and annotated CRFs. Experience with JReview is highly preferred.

Experience with Shiny, Pharmaverse, and R Markdown is preferred. Familiarity with programming languages such as Python, VBA, or C++ is a plus. Excellent analytical, problem-solving, and communication skills.

Ability to work independently while collaborating effectively within cross-functional teams. Strong organizational skills with the ability to prioritize multiple assignments and meet deadlines. Preferred Experience Experience supporting medical review or clinical data review activities.

Experience developing reusable programming utilities and automation tools. Familiarity with regulatory submission standards and clinical trial data workflows. Experience working in a fast-paced clinical development environment.

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