ZipRecruiter

Log In

2

Remote Clinical Sas Programmer Jobs in Connecticut

Experience Camps

Senior Clinical Manager

Westport, CT · On-site +1

$90K - $100K/yr

... programming, with a focus on the day-to-day coordination, support, and guidance of clinical staff ... Primarily remote position with travel for in-person requirements. On-site availability during 3-4 ...

Arvinas

Arvinas uses its proprietary PROTAC ® Discovery Engine platform to engineer proteolysis targeting ... This role can be located at our headquarters in New Haven, CT or work with a hybrid or remote work ...

Syneoshealth

Our Clinical Solutions team members act with a drug development mindset, applying their years of ... US or Canada (Hybrid/Remote) Position Overview The Research Associate/Senior Research Associate ...

next page

Showing results 1-20

All JobsClinical Sas Programmer JobsRemote Clinical Sas Programmer JobsRemote Clinical Sas Programmer Jobs in Connecticut

Remote Clinical Sas Programmer information

See Connecticut salary details

$18

$51

$76

How much do remote clinical sas programmer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for remote clinical sas programmer in Connecticut is $51.41, according to ZipRecruiter salary data. Most workers in this role earn between $39.57 and $64.71 per hour, depending on experience, location, and employer.

What does a remote SAS clinical programmer do?

The job duties of a remote SAS clinical programmer involve programming within the Statistical Analysis System (SAS) software suite. You perform your responsibilities for this virtual job from a remote location outside of your client or employer’s office. A clinical SAS programmer focuses on clinical data collection and analysis. After gathering the required dataset, you analyze the data using SAS software to find the desired information about healthcare services, clinical trials, or other similar subjects. You then document the results of the analysis.

What is a remote clinical SAS programmer?

A Remote Clinical SAS Programmer is responsible for programming, validating, and analyzing clinical trial data using SAS software while working from a remote location. They collaborate with biostatisticians and clinical teams to create datasets, generate tables, listings, and figures, and ensure compliance with regulatory standards such as CDISC, SDTM, and ADaM. Their work supports drug development and regulatory submissions, making accuracy and efficiency crucial. Strong SAS programming skills, knowledge of clinical research, and experience with regulatory guidelines are essential for this role.

What does a remote clinical SAS programmer do?

As a Remote Clinical SAS Programmer, you'll primarily support clinical trial data analysis by programming tables, listings, and figures (TLFs), creating datasets, and ensuring data integrity. You will collaborate closely with biostatisticians, data managers, and other clinical team members to provide statistical outputs for clinical study reports and regulatory submissions. Your daily tasks include writing and validating SAS code, documenting work for audit purposes, and adhering to industry standards such as CDISC. The role often involves juggling multiple projects simultaneously, offering variety and opportunities to deepen your expertise in clinical data. This environment is well-suited to self-motivated professionals seeking both autonomy and collaborative teamwork in a dynamic, impactful field.

What are the key skills and qualifications needed to thrive as a remote clinical SAS programmer?

To thrive as a Remote Clinical SAS Programmer, you need strong statistical analysis skills, proficiency in SAS programming, and a background in clinical trials or life sciences. Experience with CDISC standards, clinical databases, and regulatory compliance, as well as certifications like SAS Certification or knowledge of SDTM and ADaM, are highly valued. Attention to detail, excellent communication, and time management are critical soft skills for remote collaboration and meeting project timelines. These attributes ensure reliable data outputs, successful teamwork, and compliance with industry regulations in a remote clinical research environment.

More about Remote Clinical Sas Programmer jobs

What are the most commonly searched types of Clinical Sas Programmer jobs in Connecticut?

The most popular types of Clinical Sas Programmer jobs in Connecticut are:

What are popular job titles related to Remote Clinical Sas Programmer jobs in Connecticut?

For Remote Clinical Sas Programmer jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Sas Programmer jobs in Connecticut look for?

The top searched job categories for Remote Clinical Sas Programmer jobs in Connecticut are:

What cities in Connecticut are hiring for Remote Clinical Sas Programmer jobs?

Cities in Connecticut with the most Remote Clinical Sas Programmer job openings:

Remote Clinical Sas Programmer jobs near you
Infographic showing various Remote Clinical Sas Programmer job openings in Connecticut as of June 2026, with employment types broken down into 15% As Needed, 4% Full Time, and 81% Part Time. Highlights an 42% Physical, 2% Hybrid, and 56% Remote job distribution, with an average salary of $106,923 per year, or $51.4 per hour.

Technical Clinical Data Manager /Data Analyst (Remote)

Fairfield, CT • Remote

Penfield Search Partners
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Penfield Search Partnersexternal

Full-time

Posted 27 days ago

Job description

Contact: Neisha Camacho/Terra Parsons - 
No 3rd party candidates

We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas.

This role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. The client is seeking someone resourceful and technically curious — not just process-oriented — with the ability to independently explore datasets, generate meaningful reports, and surface potential issues early.

The ideal candidate will bring a blend of traditional clinical data management expertise along with strong data review, querying, and analytical skills. Experience with R, SQL, SAS, or other data interrogation and reporting tools is highly desirable.

Key Responsibilities

  • Support clinical data management activities across studies from start-up through database lock
  • Perform hands-on data review and exploratory analysis to identify data trends, inconsistencies, missing data patterns, and potential study risks
  • Develop custom reports, listings, and data visualizations to support proactive data cleaning and study oversight
  • Utilize R, SQL, SAS, or similar tools to query, analyze, and troubleshoot clinical datasets
  • Partner with CROs and vendors to ensure high-quality, timely data delivery
  • Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams on data review strategies and issue resolution
  • Contribute to development and review of key deliverables including:
    • Data Management Plans (DMPs)
    • eCRF design and completion guidelines
    • Edit checks and query logic
    • User Acceptance Testing (UAT)
    • Data review plans and cleaning processes
  • Support ongoing query management and ensure data integrity, consistency, and inspection readiness
  • Assist with implementation of data standards, reporting enhancements, and process improvements
  • Work independently to investigate data anomalies and recommend practical solutions in a fast-paced biotech environment

Qualifications

  • BS in a scientific, technical, or clinical discipline
  • Approximately 5–8 years of clinical data management experience within biotech, pharma, or CRO environments
  • Strong hands-on experience reviewing and interrogating clinical trial data
  • Experience using R, SQL, SAS, or other querying/reporting tools to analyze clinical data and generate custom reports
  • Experience with EDC systems such as Medidata Rave, Oracle, or Veeva
  • Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage
  • Experience supporting Phase II and/or III clinical trials; CNS experience is a plus
  • Exposure to CRO/vendor oversight
  • Understanding of clinical data structures and dictionaries including MedDRA and WHODrug
  • Strong critical thinking and problem-solving skills with the ability to work independently
  • Resourceful, proactive, detail-oriented, and comfortable operating in a dynamic biotech environment
  • Strong communication and cross-functional collaboration skills