ZipRecruiter

Log In

1

Associate Director Statistical Programming Jobs in Branchburg, NJ

Altimmune

Director, Biostatistics

Morristown, NJ · On-site

Responsible for the overall quality of statistical design, programming, analysis, and data ... A self-directed individual who can excel both independently and as a team player in a fast-paced ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site

Responsible for the overall quality of statistical design, programming, analysis, and data ... A self-directed individual who can excel both independently and as a team player in a fast-paced ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site +1

Responsible for the overall quality of statistical design, programming, analysis, and data ... A self-directed individual who can excel both independently and as a team player in a fast-paced ...

Jobtailor

Capabilities Associate Director

Raritan, NJ · On-site

$130 - $180/hr

* Being a resource to help HEMA associates navigate the organization, by providing a structured ... Understanding of HEMA analytical methods, e.g., statistics and economic modelling. * Ensure ...

New

previous page

Showing results 41-60

All JobsAssociate Statistical Programming JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Branchburg, NJ

Associate Director Statistical Programming information

See Branchburg, NJ salary details

$158.1K

$288.5K

$354.3K

How much do associate director statistical programming jobs pay per year?

As of Aug 16, 2026, the average yearly pay for associate director statistical programming in Branchburg, NJ is $288,514.00, according to ZipRecruiter salary data. Most workers in this role earn between $268,300.00 and $332,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an associate director statistical programming?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

What does an associate director statistical programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

How does an associate director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech setting?

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What cities near Branchburg, NJ are hiring for Associate Director Statistical Programming jobs?

Cities near Branchburg, NJ with the most Associate Director Statistical Programming job openings:

Associate Director Statistical Programming jobs near you
Infographic showing various Associate Director Statistical Programming job openings in Branchburg, NJ as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $288,514 per year, or $138.7 per hour.

Director, Biostatistics

Altimmune

Morristown, NJ • On-site

Full-time

Re-posted 16 days ago

Job description

About Altimmune:
Altimmune (NASDAQ: ALT) is a late clinical-stage biopharmaceutical company developing therapies for patients with serious liver diseases. The Company's lead candidate, pemvidutide, is a unique dual-action therapy targeting both glucagon and GLP-1 receptors in a balanced 1:1 ratio in development for the treatment of metabolic dysfunction-associated steatohepatitis (MASH), alcohol use disorder (AUD), and alcohol-associated liver disease (ALD). For more information, please visit
Job Position: This is a high-visibility, high-impact role that will be critical to Altimmune's growth. Reporting to the Senior Director, Biostatistics, this individual will provide statistical leadership and serve as the lead statistician for one or more clinical development programs within Altimmune's pipeline. They will work collaboratively with clinical and development teams, including clinicians, clinical scientists, statistical programmers, data managers, regulatory, and clinical operations professionals, to plan, conduct, and analyze clinical studies of all phases. Responsible for the overall quality of statistical design, programming, analysis, and data reporting. Represents the company in interactions with outside statistical and data management service providers and participates in discussions with regulatory agencies.
Workplace Designation: Depending upon location, this role will be hybrid or remote and will require some travel as business needs dictate.
Essential Functions:
Statistical Leadership
  • Serve as the lead statistician for one or more clinical development programs, providing statistic and operational leadership across all phases of clinical research.
  • Provide statistical input into development strategy, study design, sample size determination, endpoint selection, estimands, and analysis methodology.
  • Perform or oversee statistical analyses for interim study results, database locks, top-line results, and final clinical study reports.
  • Evaluate and implement innovative statistical methodologies, technologies, and AI-enabled tools to improve efficiency and quality across clinical development.
Regulatory and Documentation
  • Develop and review statistical sections of clinical protocols, Statistical Analysis Plans (SAPs), Case Report Forms (CRFs), Clinical Study Reports (CSRs), and other regulatory documents.
  • Ensure all statistical activities comply with ICH-GCP guidelines, CDISC standards, regulatory guidance, and company standards.
  • Contribute to the interpretation of clinical trial results and support the preparation of regulatory submissions, publications, scientific presentations, and responses to health authorities.
  • Represent Altimmune in interactions with external statistical vendors, CROs, and regulatory agencies.
Cross-Functional Collaboration
  • Collaborate closely with Clinical Development, Clinical Operations, Data Management, Statistical Programming, Medical Affairs, and Regulatory Affairs to ensure high-quality study design and execution.
  • Work closely with statistical programmers to ensure timely development of analysis datasets, tables, listings, and figures (TLFs) supporting clinical development and regulatory submissions.
  • Review and validate statistical programming deliverables, programmatically or through independent review, as appropriate.
  • Oversee statistical activities performed by CROs and external vendors, ensuring quality, timeliness, and compliance with regulatory requirements.
Team Development and Process Excellence
  • Foster a culture of scientific rigor, collaboration, innovation, and continuous learning within the Biometrics organization.
  • Contribute to departmental process improvements, standards development, and cross-functional initiatives that strengthen Altimmune's clinical development capabilities.
Job Requirements (Essential knowledge, skills, and attributes):
  • PhD in Statistics, Biostatistics, or related field with 7+ years of clinical trial statistics experience in biotech/pharma; or MS with 10+ years of equivalent industry
  • Strong knowledge of statistical methods relevant to clinical trials, including longitudinal data, survival analysis, and Bayesian approaches.
  • Experience with regulatory interactions and submissions, including familiarity with FDA and/or EMA expectations for statistical evidence.
  • Proficiency in SAS and/or R; extensive experience with CDISC standards (SDTM, ADaM).
  • Excellent communication and leadership skills with the ability to translate complex statistical concepts for non-statistical audiences, including clinicians, regulators, and senior leadership.
  • A self-directed individual who can excel both independently and as a team player in a fast-paced, entrepreneurial environment
  • History of successful participation within an interdisciplinary
Preferred Experience
  • Experience serving as the lead statistician for Phase 3 clinical trials and supporting NDA and/or BLA regulatory submissions is highly desirable.
  • Prior experience in metabolic diseases, liver disease, or related indications (e.g., NASH/MASH, obesity) is highly desirable
  • Experience with external control arms or synthetic cohort matching
  • Familiarity with non-invasive biomarkers and imaging endpoints

Altimmune provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Apply