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Flexible Remote Clinical Sas Programmer Jobs (NOW HIRING)

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

This role can be performed as fully remote. Our values * We believe in applying scientific rigor to ... At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical ...

Navitas Life Sciences

Senior Statistical Programmer

... clinical reporting, verification and submissions support. About the Role * Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis ...

Homeside Rehab

Remote Clinical Supervisor (OT or PT)

RI · Remote

$40/wk

As a Remote Clinical Supervisor (OT or PT) at Homeside Rehab, you will work in a fully remote setting, enjoying a flexible schedule and the opportunity to provide critical clinical supervision and ...

PharmD Live

Remote Clinical Pharmacist - Virginia

$121K - $144K/yr

Flexible | Choose your own hours | Day/Evening shifts | Monday-Friday | Weekends as needed ... TCM), Remote Patient Monitoring (RPM), and Medication Therapy Management (MTM), ensuring clinical ...

PharmD Live

Remote Clinical Pharmacist - Minnesota

$121K - $144K/yr

Clinical Pharmacist As a Clinical Pharmacist with PharmD Live, you'll engage directly with patients ... Flexible schedule * Remote work environment * Opportunities for professional growth * Supportive ...

Prosper Health

Remote Clinical Psychologist

Weston, FL · On-site +1

$100K - $120K/yr

... Flexible Work Options: * Schedule autonomy (7am-10pm - 7days a week) * Part-time/Contract roles ... Strong clinical judgment and clinical interview skills * Proficient remote communication abilities ...

Gotham Enterprises Ltd

Psychiatrist Supervisor

New Hope, PA · On-site +1

$200 - $300/hr

Psychiatrist Supervisor - New Hope, PA Join a flexible remote opportunity where your psychiatric expertise can help mental health clinicians strengthen their clinical judgement and patient care. Job ...

Rockstar

Remote Clinical Psychologist

$90K - $124K/yr

... They Offer Flexible Work Options * Schedule autonomy (7am-10pm - 7 days a week) * Part-time ... Strong clinical judgment and clinical interview skills * Proficient remote communication abilities ...

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As of Aug 8, 2026, the average hourly pay for flexible remote clinical sas programmer in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.
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Infographic showing various Flexible Remote Clinical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, and 3% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

Senior Statistical Programmer FSP

Cytel

Cambridge, MA • On-site, Remote

Full-time

Posted 17 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.

Apply