Top 62 Programmer writer Jobs in United States

Associate Director Oncology Biostatistics
Penfield Search Partners —San Francisco, CA
- 5 years
- Doctor of Philosophy
- Quality control
Quick Apply
Senior Quality Technical Specialist OH
Dayton T. Brown, Inc. —Cincinnati, OH
- $35 - $45 an hour
- Full-time
- 7 years
- Office
- Analysis skills
- Profit sharing
- Health insurance
Quick Apply
12d
Quality Technical Specialist- Cinncinati, OH
Dayton T. Brown, Inc. —Cincinnati, OH
- $25 - $35 an hour
- Full-time
- Mid-level
- Office
- 3 years
- Profit sharing
- Health insurance
Quick Apply
12d
Technical Writer
BigML —Corvallis, OR
- Remote
- Bachelor of Science
- Mid-level
- 3 years
Technical Writer
Two95 International Inc. —Roseville, CA
- Contract
- Word processing
- Research
- Mid-level
Quick Apply
SEO Content Writing
Submit Express —Glendale, CA
- $20 - $25 an hour
- Part-time
- Marketing
- 1 year
- Entry level
Technical Writer
Körber AG —Fargo, ND
- Email
- Microsoft Excel
- Microsoft Outlook
- English
- Health insurance
- Dental insurance
Technical Publications Writer
Yanmar Compact Equipment North America, Inc. —Grand Rapids, MN
- Full-time
- Engineering
- English
- Research
- Health savings account
- AD&D insurance
Quick Apply
Copywriter
iNET-Web —Waukesha, WI
- 8 hour shift
- Office
- In-person
- Internship
- Health savings account
- Health insurance
Journeyman Technical Writer
Precise Systems —Orlando, FL
- Hybrid work
- Microsoft Outlook
- Bachelor of Science
- Research
Technical Writer Level 3
Tulk LLC —St. Louis, MO
- Full-time
- Research
- Senior level
- Disability insurance
- Health insurance
Quick Apply
Documentation Specialist/Technical Writer
Connective Business Solution —Tallahassee, FL
- Full-time
- Mid-level
- 3 years
- Experience equivalent to degree accepted
Quick Apply
Product Specialist - Technical Writer
Hamilton Company —Reno, NV
- $70,000 - $110,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- 1 year
- Disability insurance
- Health insurance
IT PROGRAMMER
City of Palm Coast —Palm Coast, FL
- $69,054 - $81,368 a year
- Full-time
- Computer Science
- Writing skills
- System design
Applications Specialist/Software Quality Assurance Engineer Grades 1 - 5
Solutions Engineering —Bethesda, MD
- Bachelor of Science
- English
- Mid-level
Technical Writer - Quincy, MA
AHU Technologies Inc —Washington, DC
- $35 an hour
- Full-time
- Mid-level
- 3 years
- SharePoint
Quick Apply
Description Writer
FYI TELEVISION INC —Grand Prairie, TX
- $12 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
Lead Statistical Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Contract
- Hybrid work
- Business development
- Analysis skills
- Presentation skills
Quick Apply
Statistician
Alimentiv —Boston, MA
- $81,000 - $135,500 a year
- Email
- Remote
- Senior level
Quick Apply
11d
Electronic Technical Writer/Configuration
Our Electronics Segment —San Diego, CA
- $75,000 - $90,000 a year
- Mid-level
- 3 years
- Bachelor's degree
Quick Apply

I want to receive the latest job alert for programmer writer in united states

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

Associate Director Oncology Biostatistics

Penfield Search Partners
San Francisco, CA

Quick Apply

Job Details

Qualifications

Statistics
Statistics
Biostatistics-based research
SAS
Pharmaceutical regulatory compliance
SAS language
Data management
CDISC standards
Clinical trial support in drug product development
Technical Proficiency

Full Job Description

Our client is a clinical-stage biopharma company focusing in the Oncology space. They are currently seeking a highly skilled and experienced Associate Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. As Associate Director you will apply sound statistical methodology to meet project objectives, health authority guidelines, and regulatory requirements.

This is an onsite role based in the Bay Area.

Apply extensive technical expertise and experience to provide written and verbal recommendations on statistical issues, design and conduct of clinical trials of all phases.
Use initiative to develop, maintain and share knowledge of the theory and application of current statistical methods appropriate for data analysis and clinical trial design.
Work collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials.
Work with project team members on developing clinical protocol.
Review CRFs, CRF edit checks and CRF completion guidelines.
Author statistical analysis plan, TLF shells and Table of contents for outputs to be generated.
Review ADaM specifications and verify primary and secondary efficacy endpoints.
Perform analysis, interpret study results, and collaborate with clinical team to produce interim reports, final reports, and publications.
Effectively manage CRO to ensure high-quality deliverables within timeline and budget.
Oversee programming of ADaMs and TLFs for the study.
Responsible for one or more studies with concurrent tasks and timelines.
Participate in the validation/QC of key study endpoint analysis and submission deliverables.
Apply appropriate regulatory guidelines to the projects.
Guide the successful completion of major programs, projects and/or functions.
Develop technical and/or business solutions to complex problems.
Identify and implement methods, techniques, procedures, and evaluation criteria to achieve results.
Performs a variety of complicated tasks with a wide degree of creativity and latitude.

Please Have:

MS/MA degree in related discipline and a minimum of 9 years of related experience; or,
PhD in related discipline and a minimum of 5 years of related experience; or,
Experience in Oncology and study Phases I-III highly preferred.
Experience in Biotech/Pharmaceutical industry preferred.
Experience with managing CROs in the conduct of clinical trials.
Experience with statistical applications and clinical data management procedures in the conduct of clinical trials.
Ability to effectively represent Biostatistics and Clinical Data Management in multidisciplinary meetings.
Knowledge of appropriate regulations, industry standards and guidance documents.
Ability to interact effectively with biostatistical, data management, operations, and clinical personnel from CROs and companies collaborating with Exelixis.
Developed/reviewed SDTM/ADaM specifications
Strong SAS programming knowledge.
Complete understanding and wide application of technical principles, theories, concepts, and techniques.
Have good general knowledge of other related disciplines.

Quick Apply

Refine Your Search

programmer writer jobs in united states

Associate Director Oncology Biostatistics

Senior Quality Technical Specialist OH

Quality Technical Specialist- Cinncinati, OH

Technical Writer

Technical Writer

SEO Content Writing

Technical Writer

Technical Publications Writer

Copywriter

Journeyman Technical Writer

Technical Writer Level 3

Documentation Specialist/Technical Writer

Product Specialist - Technical Writer

IT PROGRAMMER

Applications Specialist/Software Quality Assurance Engineer Grades 1 - 5

Technical Writer - Quincy, MA

Description Writer

Lead Statistical Programmer

Statistician

Electronic Technical Writer/Configuration

I want to receive the latest job alert for programmer writer in united states

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected