Top 333 Scientific programmers Jobs

Statistical Programmer
Talentech Consulting LLC —Remote
- Contract
- Remote
- 7 years
- Computer Science
- 5 years
- Health savings account
- Health insurance
Quick Apply
Scientific Programmer
Virginia Tech —Roanoke, VA
- $73,000 - $78,000 a year
- Overtime
- Computer science
- Computer Science
- Mid-level
12d
GENETICS & GENOMICS PROGRAMMER AND DATA ANALYST, School of Medicine, Genetics, Molecular Medicine
Boston University —Boston, MA
- Mid-level
- 3 years
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12d
Research Scientist I
The Medical College of Wisconsin, Inc. —Milwaukee, WI
- Full-time
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Senior Bioinformatician
Genome International Corporation —Madison, WI
- Java
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- Senior level
Bioinformatics Programmer (100% Limited)
UCLA Health —Los Angeles, CA
- $33.96 - $69.54 an hour
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- Communication skills
Clinical Database Programmer-Reference Laboratory
Medpace, Inc. —Cincinnati, OH
- Full-time
- Office
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Research Specialist Programmer
Virginia Institute of Marine Science —Gloucester Point, VA
- Up to $20 an hour
- Temporary
- Remote
- Background check
- Computer science
- Computer Science
Project Manager - Brain Game Center
Northeastern University —Boston, MA
- $60,315.00 - $85,192.50 a year
- Full-time
- Mid-level
- 3 years
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- Health insurance
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Statistician
Alimentiv —Boston, MA
- $81,000 - $135,500 a year
- Email
- Remote
- Senior level
Quick Apply
Biostatistical Programming Manager
Amgen —Remote
- $129,056.35 - $174,605.65 a year
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Scientific Data Analyst
Alpha Omega Integration —Vienna, VA
- $85,000 - $115,000 a year
- Remote
- Mid-level
- 3 years
- Master's degree
- Health savings account
- Paid holidays
Quick Apply
Senior Bioinformatics Programmer
NYU Langone Health —New York, NY
- $84,577.92 - $105,039.78 a year
- Hybrid work
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- 3 years
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Research Scientist - Epidemiology and Scientific Affairs
Thermo Fisher Scientific —North Carolina
- $150,000 - $170,000 a year
- Full-time
- 5 years
- English
- Office
- Commuter assistance
- Paid parental leave
Scientific Programmer
Carr Astronautics Corporation —Greenbelt, MD
- Background check
- Computer science
- 7 years
Clinical Database Programmer
Medpace, Inc. —Cincinnati, OH
- Full-time
- Computer Science
- Office
- Bachelor's degree
- Paid time off
Scientific Programmer
Lynker Corporation —Silver Spring, MD
- $78,000 - $100,000 a year
- Full-time
- Remote
- 5 years
- Senior level
- Python
- Paid holidays
- Disability insurance
Sr. Principal Biostatistician
Biogen —Remote
- $134,000 - $179,000 a year
- Full-time
- 3 years
- Analysis skills
- Continuous improvement
- Paid parental leave
- Employee stock purchase plan
Bio Statistician
Katalyst Healthcares & Life Sciences —Foster, CA
- Contract
- Hybrid work
- English
- Mid-level
- Master's degree
Quick Apply
Research Assistant, Public Health-Social Sciences
Atrium Health —Winston-Salem, NC
- $30.70 - $46.05 an hour
- Full-time
- Hybrid work
- Computer literacy
- Public speaking
- Master's degree
- Paid parental leave
- Disability insurance

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Statistical Programmer

Talentech Consulting LLC
Remote

Quick Apply

Job Details

Contract

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Vision insurance
Professional development assistance

Qualifications

SAS
R
Drug regulation
SAS language
ICH guidelines
Bachelor's degree
Data management
Pharmaceutical company experience
CDISC standards
Python
Data analysis software

Full Job Description

We are looking for two experienced statistical programmers for our pharma client, this is a remote position.

Job Summary

Statistical Programming Contractor will provide oversight of CRO statistical programming activities and/or collaborate closely with other functions in the project team. Hands-on support to internal company teams and technical abilities to enable process improvements surrounding Statistical Programming will be needed, as well as hands-on support to all clinical development programs and regulatory submissions.

Roles & Responsibilities may include, but not be limited to:

1. Serve as statistical programming representative in study management teams and related regulatory interactions

2. Collaborate with biometrics and clinical development teams in building data and analysis standard

3. Ensure quality of all statistical programming deliverables

4. Review study protocol, CRF, SAP, DTAs, TFL shell and other study documentations

5. Perform / review / QC ADaMs and TFLs to ensure quality and accuracy

6. Work with Statisticians on exploratory analyses of existing data, and ongoing data query and review

7. Contribute to statistical programming deliverables for regulatory submissions

8. Develop and maintain necessary programming macros or tools to effectively support all programming needs

9. Support statistical analyses, clinical study reports, IB, regulatory related documents, publications, and scientific presentations, and perform QC activities accordingly

10. Support cross functional activities related to biometrics and clinical program development as needed

11. Other duties that may be assigned.

Supervision

Position does not have supervisory responsibilities.

REQUIREMENTS & WORKING CONDITIONS

Education & Licenses and Experience

Typically requires bachelor’s degree in computer science, statistics, or related fields and 7+ years of experience in pharmaceutical / biotechnology companies; a master’s degree related to the position may be substituted for some years of experience. Experience as a study lead programmer and / or overseeing CRO performance is required.

Competencies & Skills

· Ability to work in a fast-paced, dynamic environment with little supervision

· Expert in SAS with extensive knowledge in CDISC including SDTM, ADaM, RG, Pinnacle 21, and controlled terminologies

· Ability to prioritize and manage multiple priorities and responsibilities simultaneously and follow-through on issues in a timely manner

· Working knowledge of EDC and common Data Management applications and knowledge of other external data sources

· documentations including protocol, CRF, DTA, SAP, DDT and TFL specification

· Familiar with ICH guidelines, GCP regulations, FDA / EMA / other regulatory authority guidances related to Statistical Programming requirements.

· Strong collaboration skills

· Experience of working in start up companies, participation in regulatory interaction, leading regulatory submissions and participation in audit is preferred

· Abilities in R and/or Python are desirable, but not required.

Job Type: Contract

Benefits:

401(k)
Dental insurance
Flexible spending account
Health insurance
Health savings account
Professional development assistance
Tuition reimbursement
Vision insurance

Work Location: Remote

Quick Apply

Refine Your Search

scientific programmers jobs

Statistical Programmer

Scientific Programmer

GENETICS & GENOMICS PROGRAMMER AND DATA ANALYST, School of Medicine, Genetics, Molecular Medicine

Research Scientist I

Senior Bioinformatician

Bioinformatics Programmer (100% Limited)

Clinical Database Programmer-Reference Laboratory

Research Specialist Programmer

Project Manager - Brain Game Center

Statistician

Biostatistical Programming Manager

Scientific Data Analyst

Senior Bioinformatics Programmer

Research Scientist - Epidemiology and Scientific Affairs

Scientific Programmer

Clinical Database Programmer

Scientific Programmer

Sr. Principal Biostatistician

Bio Statistician

Research Assistant, Public Health-Social Sciences

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