Top 2717 Ema Jobs | SimplyHired

Statistical Programmer
TruMinds Technology Inc —Remote
- $100,000 - $120,000 a year
- Full-time
- Remote
- Computer Science
- Master's degree
- Bachelor's degree
Quick Apply
Former Health Agency Experts
Lachman Consultant Services —Remote
- Full-time
- Bachelor of Science
- Bachelor's degree
- Senior level
Regulatory Writing Contractor
Med Communications —Remote
- Contract
- Medicine
- Microsoft Outlook
- 5 years
Quick Apply
Temporary Clinical Research Interviewer
Syracuse University —Syracuse, NY
- $16 - $20 an hour
- Part-time
- University
- Bachelor's degree
- Psychology
Director, Healthcare Consulting - Psychometrics
Clarivate —Ann Arbor, MI
- $168,000 - $210,000 a year
- Full-time
- Remote
- Writing skills
- Analysis skills
- Bachelor's degree
- Disability insurance
- Health insurance
EU Generalist
Lachman Consultant Services —Remote
- Per diem
- Bachelor of Science
- Writing skills
- Bachelor's degree
Pharmacovigilance Associate
Puma Biotechnology —Los Angeles, CA
- $70,000 - $85,000 a year
- Weekends as needed
- Nursing
- Writing skills
- Mid-level
Adjunct Faculty - Foundations of Pharmacovigilance
MCPHS —Remote
- $2,700 - $3,000 a month
- Background check
- Mid-level
- Bachelor's degree
Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —Remote
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
Consultant, biologics CMC process development
Bionyra Pharma —Remote
- $120 - $300 an hour
- Part-time
- Remote
- 5 years
- Doctor of Philosophy
- Senior level
Quick Apply
11d
Regulatory Affairs CMC Manager
Grove —Remote
- $75 - $80 an hour
- Full-time
- Remote
- Bachelor's degree
- Doctor of Philosophy
- Senior level
Quick Apply
Clinical Scientist, Associate Director
Candel Therapeutics —Remote
- $181,000 - $194,000 a year
- Full-time
- Analysis skills
- Project management
- Continuous improvement
- Flexible schedule
6d
EDC Programmer
SystImmune —Redmond, WA
- $100,000 - $150,000 a year
- Full-time
- Hybrid work
- Computer Science
- SQL
- Bachelor's degree
- Paid holidays
- Disability insurance
Associate Director, Analytical Sciences and Attribute Characterization
Spyre Therapeutics —Remote
- $175,000 - $190,000 a year
- 8 years
- Senior level
- Leadership
- Health insurance
- Retirement plan
Medical Writer
Perceptive —Remote
- $65,305 - $93,000 a year
- Full-time
- Remote
- Nursing
- Microsoft Excel
- Mid-level
- Health savings account
- Paid holidays
11d
Vice President Regulatory Affairs
SAB —Remote
- $285,000 - $315,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Office
Quick Apply
Associate Submission and Assessment Specialist, Full-Service REMS
サイネオス・ヘルス —Remote
- $110,490 - $149,486 a year
- Remote
- Mid-level
- Bachelor's degree
- SharePoint
- Health insurance
- Dental insurance
Clinical Trial Associate/Sr. Clinical Trial Associate, Clinical Operations
Agios Pharmaceuticals —Remote
- $82,022 - $123,033 a year
- Remote
- Mid-level
- Bachelor's degree
- Continuous improvement
- Health insurance
Regulatory Associate
CEDENT —New York, NY
- Contract
- Microsoft Excel
- Mid-level
- Project management
Clinical Trial Manager, Immunology
SAB —Remote
- $150,000 - $165,000 a year
- Full-time
- Remote
- 6 years
- Bachelor of Science
- Bachelor's degree
Quick Apply
4d

I want to receive the latest job alert for ema

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

ema jobs near

Statistical Programmer

TruMinds Technology Inc
Remote

Quick Apply

Job Details

Full-time
$100,000 - $120,000 a year

Qualifications

Statistics
Clinical research
Statistics
Computer Science
R
Master's degree
Bachelor's degree
CDISC standards

Full Job Description

About the Role

Location : Remote

We are seeking a highly skilled Senior Statistical Programmer to join our growing Biometrics team. The ideal candidate will be responsible for providing advanced programming support for the analysis and reporting of clinical trial data in compliance with regulatory requirements. This role will involve working closely with Biostatisticians, Data Managers, and Clinical Teams to deliver high-quality datasets, tables, listings, and figures (TLFs).

Key Responsibilities

Develop, validate, and maintain SAS programs to generate analysis datasets (ADaM, SDTM) and TLFs for clinical trial submissions.
Ensure programming deliverables are accurate, efficient, and compliant with CDISC standards and regulatory guidelines.
Collaborate with Biostatistics and Data Management teams to understand study requirements and timelines.
Participate in the development of programming standards, macros, and process improvements.
Provide mentorship and guidance to junior programmers and review their work for quality and accuracy.
Support regulatory submissions (FDA, EMA, PMDA) by preparing submission-ready datasets and documentation.
Troubleshoot and resolve complex programming issues independently.

Qualifications

Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
9+ years of experience as a Statistical Programmer in the pharmaceutical, biotechnology, or CRO industry.
Strong proficiency in SAS programming; knowledge of R or other statistical software is a plus.
In-depth knowledge of CDISC SDTM and ADaM standards.
Experience supporting Phase I–IV clinical trials and regulatory submissions.
Excellent problem-solving, communication, and organizational skills.
Ability to work both independently and in a team-oriented environment.

Preferred Qualifications

Experience with eCTD submissions and regulatory agency interactions.
Familiarity with oncology, rare disease, or other therapeutic areas.
Knowledge of data visualization tools (e.g., R Shiny, Spotfire).

Job Type: Full-time

Pay: $100,000.00 - $120,000.00 per year

Experience:

SAS: 4 years (Preferred)
R Programmer: 1 year (Preferred)

Location:

Remote (Required)

Work Location: Remote

Quick Apply

Refine Your Search

ema jobs

Statistical Programmer

Former Health Agency Experts

Regulatory Writing Contractor

Temporary Clinical Research Interviewer

Director, Healthcare Consulting - Psychometrics

EU Generalist

Pharmacovigilance Associate

Adjunct Faculty - Foundations of Pharmacovigilance

Regulatory Writer and/or Regulatory QC/ Editor

Consultant, biologics CMC process development

Regulatory Affairs CMC Manager

Clinical Scientist, Associate Director

EDC Programmer

Associate Director, Analytical Sciences and Attribute Characterization

Medical Writer

Vice President Regulatory Affairs

Associate Submission and Assessment Specialist, Full-Service REMS

Clinical Trial Associate/Sr. Clinical Trial Associate, Clinical Operations

Regulatory Associate

Clinical Trial Manager, Immunology

I want to receive the latest job alert for ema

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected