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Senior Statistical Programmer Jobs in Miami, FL (NOW HIRING)

... Level Senior Associate & Summary At PwC, our people in data and analytics engineering focus on ... You will work on developing predictive models, conducting statistical analysis, and creating data ...

The Sr. Technical Staff Engineer on the Technical Services team will be responsible for providing ... Statistical Analysis. PHYSICAL DEMANDS : Occasional bending, twisting, and lifting of twenty-five ...

The Sr. Technical Staff Engineer on the Technical Services team will be responsible for providing ... Statistical Analysis. PHYSICAL DEMANDS : Occasional bending, twisting, and lifting of twenty-five ...

The Sr. Technical Staff Engineer on the Technical Services team will be responsible for providing ... Statistical Analysis. PHYSICAL DEMANDS : Occasional bending, twisting, and lifting of twenty-five ...

Design and implement advanced ML models and statistical methods to optimize forecasting, risk ... Azure Data Scientist Associate, or TensorFlow Developer Certification. Security clearance: * Active ...

About the Role We are looking for a seasoned Senior Data Scientist to join our Analytics team to ... Experience with statistical modeling and data analysis using programming languages such as Python.

About the Role We are looking for a seasoned Senior Data Scientist to join our Analytics team to ... Experience with statistical modeling and data analysis using programming languages such as Python.

About the Role We are looking for a seasoned Senior Data Scientist to join our Analytics team to ... Experience with statistical modeling and data analysis using programming languages such as Python.

Overview As a Senior Data Engineer, you will play a pivotal role in driving our data strategy and ... Utilize tools such as Jupyter, SQL, dashboards, statistical analysis, and data visualizations to ...

This Opportunity WSP is currently initiating a search for a Senior Structural Engineer for our ... statistical analysis, and reporting. * Assist with development and scoping of medium-sized projects.

Senior Structural Engineer (Buildings)

Miami Lakes, FL · On-site

$91K - $123K/yr

This Opportunity WSP is currently initiating a search for a Senior Structural Engineer for our ... statistical analysis, and reporting. * Assist with development and scoping of medium-sized projects.

Showing results 21-40

Senior Statistical Programmer information

See Miami, FL salary details

$78.8K

$122.5K

$159.9K

How much do senior statistical programmer jobs pay per year?

As of Aug 20, 2026, the average yearly pay for senior statistical programmer in Miami, FL is $122,509.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,200.00 and $141,300.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

What are the key skills and qualifications needed to thrive as a senior statistical programmer, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the most commonly searched types of Statistical Programmer jobs in Miami, FL?

The most popular types of Statistical Programmer jobs in Miami, FL are:

What are popular job titles related to Senior Statistical Programmer jobs in Miami, FL?

For Senior Statistical Programmer jobs in Miami, FL, the most frequently searched job titles are:

What job categories do people searching Senior Statistical Programmer jobs in Miami, FL look for?

The top searched job categories for Senior Statistical Programmer jobs in Miami, FL are:

What cities near Miami, FL are hiring for Senior Statistical Programmer jobs?

Cities near Miami, FL with the most Senior Statistical Programmer job openings:

Infographic showing various Senior Statistical Programmer job openings in Miami, FL as of August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution, with an average salary of $122,509 per year, or $58.9 per hour.

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL • On-site

$99K - $136K/yr

Full-time

Re-posted 8 days ago


Job description

Position Summary

The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.

Essential Duties and Responsibilities

  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications

  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications

  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?

We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.