Top 5 Sas/biostatistician programmer Jobs in Boston, Ma

Lead Statistical Programmer
Katalyst Healthcares & Life Sciences —Boston, MA
- Contract
- Hybrid work
- Business development
- Analysis skills
- Presentation skills
Quick Apply
Statistical Programming Associate Director
Sumitomo Pharma America, Inc. —Marlborough, MA
- $168,000 - $210,000 a year
- Full-time
- Bachelor of Science
- Pass drug screening
- Office
- Paid holidays
- Health insurance
Principal Statistical Programmer
Vertex Pharmaceuticals —Boston, MA
- $149,200 - $223,800 a year
- Full-time
- Bachelor of Science
- Writing skills
- 8 years
- Loan repayment program
- Dental insurance
Executive Director, Biostatistics
Sarepta Therapeutics —Cambridge, MA
- $256,000 - $320,000 a year
- Full-time
- Hybrid work
- 11+ years
- Master's degree
- Analysis skills
Director, Biostatistics
Treeline Biosciences —Watertown, MA
- $226,425 - $257,000 a year
- Office
- 3 years
- Doctor of Philosophy
Quick Apply
8d

I want to receive the latest job alert for sas/biostatistician programmer in boston, ma

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

sas/biostatistician programmer jobs near boston, ma

Lead Statistical Programmer

Katalyst Healthcares & Life Sciences -
Boston, MA

Quick Apply

Job Details

Contract

Qualifications

Research project team leadership
Software project management
Statistics
Biostatistics
SAS
Team leadership
Presentations for conferences or internal meetings
Drug regulation
FDA 21 CFR Part 11
SAS language
Team development
Schedule management
Business development
Research project technical leadership
ICH guidelines
Clinical research compliance
Records management
CDISC standards
Managing clinical research teams
Mentoring
Leading team collaboration initiatives
Software development
Managing projects
Pharmaceutical research experience
Technical Proficiency
Data analysis software
Stakeholder management
Database software proficiency

Full Job Description

Responsibilities:

Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Assist in establishing standardized programming procedures and work instructions.
Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
Develop and maintain clinical processing workflow systems.
Assist in the development of client proposal documents.
Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.) records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards).
Assist in updating/writing PROMETRIKA standard operating procedures (SOPs).
Develop tools in SAS for data analysis and reporting that comply with regulatory requirements.
Develop specifications (e.g., metadata files), annotate CRFs and create SAS programs for the mapping of raw datasets to CDISC SDTM standards.
Create define.xml files from metadata files for SDTM and ADaM.
Convert data received in other formats to SAS datasets.

Requirements:

Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS.
Knowledge of SDTM, ADaM, FDA and ICH guidance.
Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
Consistent experience as a lead statistical programmer on several concurrent projects.
Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
Excellent analytical skills.
Proven ability to learn new systems and function in an evolving technical environment.
Ability to negotiate and influence to achieve results.
Good presentation skills.
Good business awareness/business development skills (including financial awareness).
Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
Work effectively in a quality-focused environment.
Knowledge of other programming languages and database management software packages is a plus.

Quick Apply

Refine Your Search

sas/biostatistician programmer jobs in boston, ma

Lead Statistical Programmer

Statistical Programming Associate Director

Principal Statistical Programmer

Executive Director, Biostatistics

Director, Biostatistics

I want to receive the latest job alert for sas/biostatistician programmer in boston, ma

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected