1

Sas Programming Manager Jobs in Bloomfield, NJ (NOW HIRING)

Must possess expertise in SAS and clinical trial programming including data steps, procedures, SAS ... Familiarity with clinical data management concepts. * Effective interpersonal skills and ability to ...

Relevant clinical development experience (programming, RBM/RBQM, Data Management), for example: o PhD: 3+ years o MS: 5+ years o BA/BS: 8+ years Technical - Required * Advanced SAS programming skills ...

We deliver strategic workforce solutions that help you manage your talent and business more ... focus SAS Skill Competencies: Accessing Data Creating Data Structures Managing Data Generating ...

Showing results 21-40

Sas Programming Manager information

See Bloomfield, NJ salary details

$15

$50

$81

How much do sas programming manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for sas programming manager in Bloomfield, NJ is $50.16, according to ZipRecruiter salary data. Most workers in this role earn between $35.19 and $62.98 per hour, depending on experience, location, and employer.

What is a SAS programming manager?

SAS Programming Managers are professionals who oversee teams of SAS programmers, typically within the pharmaceutical, clinical research, or data analytics industries. Their responsibilities include project management, team leadership, and ensuring quality standards for statistical programming deliverables. They coordinate with other departments, manage timelines, and ensure that all data analysis and reporting using the SAS software adhere to regulatory and organizational requirements.

What are some typical challenges faced by a SAS programming manager when leading a team of programmers in a clinical research setting?

A SAS Programming Manager in clinical research often encounters challenges such as balancing tight project timelines with data quality standards, coordinating cross-functional communication between statisticians, data managers, and regulatory teams, and ensuring team members stay updated on evolving industry regulations (like CDISC standards). Managing a diverse team with varying experience levels also requires strong mentorship and effective delegation to ensure consistent deliverables. Addressing these challenges proactively helps maintain project momentum and fosters professional growth within the team.

What are the key skills and qualifications needed to thrive as a SAS programming manager, and why are they important?

To thrive as a SAS Programming Manager, you need advanced SAS programming expertise, a solid background in statistics or data analysis, and typically a degree in a quantitative field with relevant management experience. Familiarity with clinical data management systems, regulatory standards (such as CDISC), and tools like SAS Base, Macro, and SQL is essential. Strong leadership, project management, and communication skills help you effectively lead teams and collaborate across departments. These competencies ensure the delivery of high-quality data outputs, regulatory compliance, and the successful management of complex projects.

What is the difference between Sas Programming Manager vs Sas Developer?

AspectSas Programming ManagerSas Developer
CredentialsBachelor's or Master's in Computer Science, Statistics, or related field; SAS certifications often preferredBachelor's in similar fields; SAS certifications beneficial
Work EnvironmentLeads teams, manages projects, collaborates with stakeholdersDevelops SAS programs, analyzes data, implements solutions
Industry UsageUsed in healthcare, finance, pharma for project oversightUsed across industries for data analysis and reporting
Search & ComparisonOften compared for leadership roles in SAS programmingFocuses on coding and data analysis tasks

The Sas Programming Manager oversees SAS projects and manages teams, while the Sas Developer primarily focuses on coding and data analysis. Both roles require SAS skills and certifications, but the manager role involves leadership and project management responsibilities, whereas the developer role emphasizes technical programming tasks.

What cities near Bloomfield, NJ are hiring for Sas Programming Manager jobs?

Cities near Bloomfield, NJ with the most Sas Programming Manager job openings:

Infographic showing various Sas Programming Manager job openings in Bloomfield, NJ as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $104,338 per year, or $50.2 per hour.

Senior Scientist, Statistical Programming

MSD Malaysia

Rahway, NJ โ€ข On-site

$117 - $184/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago


Key responsibilities

  • Support statistical programming activities for late-stage drug/vaccine clinical development projects.

  • Develop and execute statistical analysis and reporting deliverables such as datasets, tables, listings, and figures.

  • Design and maintain statistical datasets to support multiple stakeholder groups and ensure project plans are executed efficiently with high-quality deliverables.


Job description

Senior Scientist, Statistical Programming โ€“ Rahway, NJ: Provide support to statistical programming activities for late-stage drug/vaccine clinical development projects. Be accountable for the development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. Design and maintain statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation. Act as a key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high quality deliverables. Serve as the statistical programming point of contact and knowledge holder through the entire product lifecycle. Apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Lead one or more projects.

Requirements:
  • Must have a Masterโ€™s degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years experience in SAS programming in a clinical trial environment OR a Bachelorโ€™s degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years experience in SAS programming in a clinical trial environment.
  • Experience in CDISC and ADaM standards.
  • Experience in designing and developing complex programming algorithms and ensuring process compliance and deliverable quality.
  • Must possess expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH. Systems and database expertise.
  • Must have ability to comprehend analysis plans which may describe methodology to be programmed.
  • Have an understanding of statistical terminology and concepts; strategic thinking ability to turn strategy into tactical activities.
  • Ability to design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices.
  • Ability to anticipate stakeholder requirements.
  • Familiarity with clinical data management concepts.
  • Effective interpersonal skills and ability to negotiate and collaborate effectively.
  • Written, oral, and presentation skills.
  • Knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings) also required.
  • Must be a project leader and possess ability to complete tasks independently at a project level.
  • Ability to collaborate with key stakeholders.
Required Skills:
  • Clinical Development
  • Clinical Trials
  • Computer Science
  • Data Management
  • Data Modeling
  • Global Health
  • Marketing
  • Numerical Analysis
  • Outcomes Research
  • Project Leadership
  • Stakeholder Engagement
  • Stakeholder Relationship Management
  • Statistical Analysis
  • Statistical Programming
  • Strategic Thinking
  • Waterfall Model
  • Working Independently

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anotherโ€™s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employeeโ€™s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angelesโ€™ Fair Chance Initiative for Hiring Ordinance

Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 11/1/2026 A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

#J-18808-Ljbffr