Remote jobs in the United States

22 jobs

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Added 21 hours ago
Statistics Leader/Associate Director, Medical & Market Access Oncology Statistics
GlaxoSmithKline Services Unlimited
Remote, United States
· Practical experience with statistical programming and simulations using R, Python, SAS or similar tools.
Added 3 days ago
Associate Director, Biostatistics
BeOne Medicines USA, Inc.
Remote, United States
Regulatory, Statistical Programming, Data Management and other Research Scientists in reviewing the data,
Added 3 days ago
Senior Manager, Statistical Programming
EDETEK
Remote, United States
Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.
Added 5 days ago
AP
Associate Director, Medical Affairs Statistical Sciences (Biometrics) - ID: 2069
Ascendis Pharma
Remote, United States
- $200,000 to $215,000 USD / year
The Associate Director, Medical Affairs Statistical Sciences Biometrics provides technical and operational support for the design, implementation and interpretation of post approval…
Added 10 days ago
Associate Director, Statistical Programming
Tyra Biosciences
Remote, United States
Tyra Biosciences, Inc. is seeking a highly motivated Associate Director, Statistical Programming, to make impactful contributions to projects targeting disease areas with high unmet medical…
Added 15 days ago
Associate Director, Biostatistics FSP
Cytel
Remote, United States
As an Associate Director of Biostatistics, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to support or lead clinical trials for drug…
Added 15 days ago
Associate Director, Biostatistics FSP
Cytel
Remote, United States
As an Associate Director of Biostatistics, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to support or lead clinical trials for drug…
Added 21 days ago
Associate Director, Medical Affairs Statistical Sciences (Biometrics) - ID: 2069
Ascendis Pharma
Remote, United States
The Associate Director, Medical Affairs Statistical Sciences Biometrics provides technical and operational support for the design, implementation and interpretation of post approval…
Added 21 days ago
Senior Manager, Statistical Programming
EDETEK
Remote, United States
Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.
Added 24 days ago
Associate Director, Programming
Insmed Incorporated
Remote, United States
We’re looking for an Associate Director, Programming to help us expand what’s possible for patients with serious diseases. Reporting to the Executive Director, Head of Programming, you’ll…
Added 1 month ago
Associate Director, Biostatistics
Jazz Pharmaceuticals, Inc.
Remote, United States
The Associate Director, Biostatistics will function as the statistical lead on a Jazz Pharmaceuticals drug development project or as the statistical lead for individual clinical trials,…
Added 1 month ago
Associate Director, Biostatistics
RayzeBio, Inc
Remote, United States
The Associate Director of Biostatistics at RayzeBio will play a crucial role in guiding the design, execution, and interpretation of statistical analyses for clinical trials, with the…
Added 1 month ago
Associate Director, Biostatistics
BeOne Medicines USA, Inc.
Remote, United States
Regulatory, Statistical Programming, Data Management and other Research Scientists in reviewing the data,
Added 1 month ago
Associate Director, Biostatistics FSP
Cytel
Remote, United States
As an Associate Director of Biostatistics, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to support or lead clinical trials for drug…
Added 1 month ago
Associate Director, Biostatistics FSP
Cytel
Remote, United States
As an Associate Director of Biostatistics, you will be dedicated to one of our FSP clients, working as an extension of their staff to support or lead clinical trials for drug development,…
Added 1 month ago
Associate Director, Real-World Analytics Programming
Revolution Medicines
Remote, United States
Independently develops, validates, and maintains SAS, SQL, R, Python, and other programming solutions for cohort construction, endpoint derivation, analysis dataset creation, and study…
Added 1 month ago
Senior Manager/Associate Director, Biostatistics
Rapport Therapeutics
Remote, United States
Rapport is seeking a Senior Manager / Associate Director of Biostatistics who will have a hands-on role in shaping the design, analysis, and interpretation of clinical trial data for our…
Added 1 month ago
Associate Director, Biostatistics
Oruka Therapeutics
Remote, United States
The Associate Director of Biostatistics will provide statistical leadership and operational execution for clinical development programs and individual clinical trials. This individual will…
Added 1 month ago
Associate Director, Expert EPI Programmer
Cytel
Remote, United States
The Associate Director, Epidemiological Statistical Programming serves as a senior technical leader within the Epidemiology programming function, providing functional guidance, technical…
Added 1 month ago
Associate Director/Director of Statistical Programming
BridgeBio Pharma
Remote, United States
The Director of Statistical Programming will lead statistical programming activities for multiple studies and programming submission-related activities. In addition to working as a hands-on…
Added 1 month ago
Associate Director, Biostatistics & AI
BridgeBio Pharma
Remote, United States
The Associate Director, Biostatistics & AI is a senior individual contributor and emerging people leader responsible for the delivery of high-quality statistical analyses and for designing,…
Added 1 month ago
Associate Director/Director, Data Management
Codera
Remote, United States
The Director or Associate Director, Data Management supports the Data Management (DM) department and all clinical development programs. This individual is responsible for Electronic Data…

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EDETEK

Senior Manager, Statistical Programming

Remote, United States

Apply on apply.workable.com About employer

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Job details

Experience: At least 2 years of clinical SAS programming experience for the manager position.
Posting language: English
Posted: Oct 22, 2026

Original job description

The Senior Manager of Statistical Programming will stay hands-on with daily activities of a Statistical Programmer or Sr. Statistical Programmer. He/she

Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR);
Acts as lead programmer for assigned projects;
Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies;
Writes code using Base SAS programs, SAS procedures, or standardized macros;
Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data;
Performs data checks as needed, to ensure integrity and correctness of data displays;
Prepares documentation for programs;
Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole;
Creates SAS datasets of clinical data from clinical databases;
Creates status and efficacy datasets;
Creates project-specific macros and formats;
Loads client data from other platforms and other software packages;
Prepares data to be sent to clients and as needed for other external transfers and data imports.

In addition to above job duties, Senior Manager of Statistical Programming also

Communicates with clients to set and manage project timelines and deliverables;
Assigns projects to the team and solves problems and/or technical difficulties;
Trains junior team members on industry regulations, standards and internal tools used;
Works with IT department to setup and ensure a secure environment with proper access control on SAS servers;
Works with Quality Assurance team on Standard Operation Procedures drafting and revision, as well as testing and validation of CONFORM modules.

Requirements

Ability to communicate effectively in English, in both writing and verbal.
Ability to learn quickly and pay attention to details.
Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries.
Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients.
Ability to work independently, takes ownership and strives for quality and efficiency.
Ability to work positively in a continually changing environment.
Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.
Master’s degree or above in Biostatistics, Computer Science, Mathematics, or a combination of education and relevant industry experience.
Strong SAS programming language and good knowledge/experiences of clinical trial and drug development.
At least 2 years of clinical SAS programming experience for the manager position.
Some travel (5%) may be required with a potential of travel occurring over weekends.
Cross-functional interactions

Note on Position Level:

We are open to considering qualified candidates at the Senior Manager, Associate Director, Director level, or above, depending on experience and qualifications.

Benefits

Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees.

Choice of comprehensive Medical, Vision and Dental Insurance plans
Paid vacation time and sick days
Corporate holidays annually
Participation in the 401K Plan
Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc.
Health Advocate and Employee Assistance Program

Location This position is open to onsite, hybrid, or remote candidates within the United States. Equal Opportunity Employer Statement EDETEK is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment on the basis of an individual’s race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Whenever possible, the company makes reasonable accommodations for qualified individuals with disabilities to the extent required by law.

Apply on apply.workable.com About employer

More about this job

Skills

Corporate social responsibility
Statistics
SAP
Clinical research
SAS
Documentation
Quality assurance
Work independently
Reporting
Computer science

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Work requirements

Remote jobs in the United States