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Senior Manager Statistical Programming Jobs in Raleigh, NC

Provide endtoend statistical programming support for clinical studies from study setup through ... Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

Provide endtoend statistical programming support for clinical studies from study setup through ... Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

Provide endtoend statistical programming support for clinical studies from study setup through ... Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

Provide end-to-end statistical programming support for clinical studies from study setup through ... Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

Provide end-to-end statistical programming support for clinical studies from study setup through ... Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

Provide endtoend statistical programming support for clinical studies from study setup through ... Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

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Senior Manager Statistical Programming information

See Raleigh, NC salary details

$23.3K

$96.2K

$162.3K

How much do senior manager statistical programming jobs pay per year?

As of Jun 9, 2026, the average yearly pay for senior manager statistical programming in Raleigh, NC is $96,244.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,600.00 and $104,000.00 per year, depending on experience, location, and employer.

What are Senior Manager Statistical Programming?

A Senior Manager Statistical Programming is a leadership role in the field of clinical research and biostatistics, typically within the pharmaceutical, biotechnology, or contract research organization (CRO) industries. This professional oversees teams of statistical programmers responsible for analyzing clinical trial data, ensuring data accuracy, and delivering high-quality statistical outputs for regulatory submissions. The role involves project management, resource allocation, mentoring staff, and collaborating with cross-functional teams to ensure compliance with regulatory standards and timelines.

What is the difference between Senior Manager Statistical Programming vs Statistical Programmer?

AspectSenior Manager Statistical ProgrammingStatistical Programmer
CredentialsBachelor's/Master's in Biostatistics, Computer Science, or related field; often with management experienceBachelor's or Master's in Biostatistics, Statistics, or related field
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms data analysis, programming, and validation tasks under supervision
Employer & Industry UsagePharmaceutical, biotech companies, CROs, clinical researchPharmaceutical, biotech, clinical research organizations

The main difference is that Senior Manager Statistical Programming oversees teams and manages projects, while Statistical Programmers focus on executing data analysis and programming tasks. The senior role involves leadership responsibilities, whereas the programmer role is more technical and task-oriented.

What are the key skills and qualifications needed to thrive as a Senior Manager Statistical Programming, and why are they important?

To thrive as a Senior Manager Statistical Programming, you need expertise in biostatistics, programming languages like SAS or R, and experience with clinical trial data, typically supported by an advanced degree in a quantitative field. Familiarity with regulatory requirements (e.g., CDISC standards), clinical data management systems, and project management tools is essential. Strong leadership, communication, and problem-solving skills help you lead teams and liaise with cross-functional stakeholders. These skills ensure accurate, compliant data analyses and effective team management for successful clinical trial outcomes.

How does a Senior Manager Statistical Programming typically collaborate with cross-functional teams in clinical research projects?

A Senior Manager Statistical Programming plays a pivotal role in coordinating with biostatisticians, clinical data managers, and medical writers to ensure seamless data flow and analysis throughout clinical trials. They oversee programming teams to deliver statistical outputs, such as tables, listings, and figures, while maintaining compliance with regulatory standards. Regular meetings and clear communication are essential, as the Senior Manager must interpret project requirements and translate them into actionable programming tasks, ensuring timelines and quality standards are met. This collaborative environment fosters continuous learning and problem-solving, as cross-functional input is vital for addressing complex data challenges.
What are popular job titles related to Senior Manager Statistical Programming jobs in Raleigh, NC? For Senior Manager Statistical Programming jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Senior Manager Statistical Programming jobs in Raleigh, NC look for? The top searched job categories for Senior Manager Statistical Programming jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Senior Manager Statistical Programming jobs? Cities near Raleigh, NC with the most Senior Manager Statistical Programming job openings:
Infographic showing various Senior Manager Statistical Programming job openings in Raleigh, NC as of May 2026, with employment types broken down into 100% Full Time. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $96,244 per year, or $46.3 per hour.
Sr. Director, Statistical Programming Safety

Sr. Director, Statistical Programming Safety

Penfield Search Partners

Raleigh, NC • Hybrid

Other

Posted 5 days ago


Job description

Job Description Contact: Lauren Scutero - lscutero@penfieldsearch.com This is a permanent, hybrid position in Raleigh, NC with two days (Monday, Friday) as optional work from home with core collaboration days in the office: Tues, Wed, Thurs. Fully home-based work is not available for this role. Job Description Position Summary Provides strategic, operational, and hands on (player coach) leadership for compound level safety statistical programming and aggregate safety reporting deliverables, including DSUR, PSUR/PBRER, Risk Management Plan (RMP), IBRSI, and support for broader safety surveillance and safety analytics

Leads teams and oversees vendors to ensure timely, high quality, and inspection ready delivery while driving modernization through AI enabled and automated programming approaches. Key Responsibilities Lead end to end programming strategy and execution for compound level aggregate safety reporting deliverables (DSUR, PSUR/PBRER, RMP, IBRSI). Provide strategic oversight of roles, responsibilities, and build steps for aggregate safety programming delivery.

Serve as escalation point for complex pooled/cumulative safety analyses and urgent ad hoc safety requests. Maintain hands on engagement to ensure technical correctness, reproducibility, and delivery reliability for critical outputs. Ensure consistent processes, folder structures, and operational readiness for safety programming deliverables.

Own and continuously improve quality management practices, including definition and monitoring of KPIs. Provide vendor/FSP oversight and governance, ensuring training readiness, documented expectations, and appropriate QC. Lead, mentor, and develop Safety Statistical Programming staff; oversee less experienced colleagues and contribute to development of standards, tools, and templates.

Drive adoption of AI enabled and automated programming approaches to improve efficiency, consistency, and quality. Capabilities & Requirements Excellent written and verbal communication; strong influencing and negotiation skills. Deep knowledge of drug development, regulatory expectations, and industry standards for safety programming and reporting.

Proven ability to lead people leaders, delegate effectively, coach performance, and support career development. Strong judgment and problem solving skills in complex situations; ability to prioritize critical issues. Demonstrated ability to work cross functionally and influence decision making.

Education & Experience Bachelor's degree or higher in Biostatistics, Computer Science, or related field with 12+ years of relevant industry experience. 6+ years of leadership or cross functional project management experience, including managing project teams. Significant line management experience with a proven record of hiring and developing high performing talent.

Extensive experience with SAS; experience with R and/or Python preferred. Demonstrated leadership in change management and standards adoption.