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Clinical Statistical Programmer Jobs in Connecticut

Performs statistical analysis and presents results. * Compose engineering reports. * Research ... Participation in pre-clinical in vivo labs, observing cases in hospitals and through customer ...

Performs statistical analysis and presents results. * Compose engineering reports. * Research ... Participation in pre-clinical in vivo labs, observing cases in hospitals and through customer ...

Performs statistical analysis and presents results. * Compose engineering reports. * Research ... Participation in pre-clinical in vivo labs, observing cases in hospitals and through customer ...

Performs statistical analysis and presents results. * Compose engineering reports. * Research ... Participation in pre-clinical in vivo labs, observing cases in hospitals and through customer ...

Knowledge of statistical software packages (e.g. Minitab) and applications. Understanding of ISO ... Awareness of clinical and regulatory pathways, IP and internal processes. EDUCATION: Minimum of B.S ...

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

... clinical outcomes, customer satisfaction and business value for all commercialized Surgical ... Ability to apply statistical methods and science-based decisions to design experiments and ...

... clinical outcomes, customer satisfaction and business value for all commercialized Surgical ... Ability to apply statistical methods and science-based decisions to design experiments and ...

Showing results 21-40

Clinical Statistical Programmer information

See Connecticut salary details

$15

$51

$85

How much do clinical statistical programmer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical statistical programmer in Connecticut is $51.54, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $77.50 per hour, depending on experience, location, and employer.

What does a clinical statistical programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What does a clinical statistical programmer do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

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

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What are some common challenges faced by clinical statistical programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are popular job titles related to Clinical Statistical Programmer jobs in Connecticut?

For Clinical Statistical Programmer jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Clinical Statistical Programmer jobs in Connecticut look for?

The top searched job categories for Clinical Statistical Programmer jobs in Connecticut are:

What are popular job titles related to Clinical Statistical Programmer jobs in CT?

For Clinical Statistical Programmer jobs in CT, the most frequently searched job titles are:

Infographic showing various Clinical Statistical Programmer job openings in Connecticut as of August 2026, with employment types broken down into 3% As Needed, 70% Full Time, 16% Part Time, 2% Temporary, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $107,205 per year, or $51.5 per hour.

R-D Engineer II

Medtronic

North Haven, CT • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Medtronic rating

7.8

Company rating: 7.8 out of 10

Based on 178 frontline employees who took The Breakroom Quiz

175th of 542 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 28 Aug 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
The R&D Engineer II will join the Wound Management R/D Engineering COE and play a key role in new product development and lifecycle support of wound closure products. This position will contribute to the design and development of surgical sutures, and enabling technologies, working closely with NPD core teams to translate customer needs into safe, effective, and commercially successful products. This role offers the opportunity to make a direct impact on patient outcomes through the advancement of world-class wound closure solutions.
Surgical Innovations
Our teams work on advancing the science and practice of surgery through technologies that enable safer procedures, improved clinical outcomes, and better experiences for both patients and healthcare providers. From concept through commercialization, we combine engineering excellence, clinical insight, and manufacturing expertise to bring life-changing medical technologies to market.
By fostering a culture of innovation, collaboration, and continuous improvement, we help shape the future of surgery and delivering on Medtronic's mission to alleviate pain, restore health, and extend life.
Responsibilities may include the following and other duties as assigned:
  • Designs, develops, analyzes, troubleshoots, and provides technical skills during research and/or product development.
  • Designs studies to investigate root cause or identify process parameters.
  • Supports product development activities.
  • Provides feedback on machine design and prototypes.
  • Designs fixturing for manufacturing equipment or testing.
  • Creates prototype test samples.
  • Supports the voice of customer and pre-clinical studies.
  • Prepares and tracks test samples.
  • Assists in DOE planning and execution.
  • Performs statistical analysis and presents results.
  • Compose engineering reports.
  • Research technical and procedural topics and reports of findings to groups.
  • Work will be performed in R&D laboratories and in manufacturing facilities.

Required Knowledge and Experience:
  • Requires a Baccalaureate degree in Materials Science & Engineering, Mechanical Engineering, or Biomedical Engineering and minimum of 2 years of relevant experience OR Master's degree with a minimum of 0 years relevant experience.
  • Self-motivated and proactive, with the ability to take ownership of assignments and drive work forward with appropriate guidance
  • Demonstrates emerging leadership potential through influence, accountability, strong communication, and a willingness to lead technical activities and project deliverables.

Nice to Have
  • Specialization in absorbable polymers, surgical needles, or sutures
  • Experience in the medical device industry
  • Practical experience and theoretical knowledge in the one or more of the following areas:
    • Polymer development and manufacturing
    • Fiber extrusion
    • Textile manufacturing
    • Material characterization
    • Sterile barrier packaging design for medical devices
    • High volume manufacturing assembly processes
  • Ability to apply statistical methods and science-based decisions to design experiments and implement improvements
  • Demonstrated ability to deliver quality technical work within project schedules and timelines. Ability to work in a fast-paced, deadline driven environment.
  • Must be team oriented, with the ability to work well on common deliverables with diverse cross-functional teams and to interact at the highest professional manner with all organizational levels
  • Excellent communication skills, both verbal and written, and interpersonal skills to successfully partner on varying levels ranging from cross functional to global multi-site and multi-business unit
  • Participation in pre-clinical in vivo labs, observing cases in hospitals and through customer interactions.
  • Demonstrated ability to manage and prioritize multiple tasks/projects with a strong problem-solving ability.
  • Experience with DRM / DFSS, Lean Sigma, or Green/Black Belt Lean Sigma certification
  • Knowledge of Microsoft applications (Excel, Word, Outlook, Powerpoint)
  • Excellent communication skills, both verbal and written, and interpersonal skills to successfully partner on varying levels ranging from cross functional to global multi-site and multi-business unit

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD):$88,800.00 - $133,200.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

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