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Associate Director Statistical Programming Jobs in Campbell, CA

RXinsider LTD.

Associate Director Engineering

Milpitas, CA · On-site

$183.80 - $294.10/hr

Position Summary The Associate Director of Engineering is the senior engineering leader at the site level, responsible for engineering execution, technical governance, and performance. This role ...

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All JobsAssociate Statistical Programming JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Campbell, CA

Associate Director Statistical Programming information

See Campbell, CA salary details

$177.7K

$324.2K

$398.1K

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

As of Aug 9, 2026, the average yearly pay for associate director statistical programming in Campbell, CA is $324,245.00, according to ZipRecruiter salary data. Most workers in this role earn between $301,500.00 and $373,300.00 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 Campbell, CA are hiring for Associate Director Statistical Programming jobs? Cities near Campbell, CA 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 Campbell, CA 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 $324,245 per year, or $155.9 per hour.

Director, Biostatistics

Summit Therapeutics

Palo Alto, CA

Full-time

Re-posted 9 days ago

Job description

Overview of Role:

Serves as the project level biostatistician and provides leadership within biostatistics function to develop and execute statistical strategy, study design, statistical analyses, and regulatory submissions for clinical trials in oncology. Partners with clinical science, regulatory and other team members in clinical development plans, authoring key clinical/regulatory/statistical documents, and ensuring exceptional delivery and interpretation of clinical data. Develops and implements biostatistics department policies, standards, procedures, and work-instructions in coordination with department leader and other functions. Represents biostatistics function in interactions with CROs, institutional review boards, and regulatory agencies.

Role and Responsibilities:

  • Provide technical leadership and statistical support to clinical development through the design and conduct of clinical studies in oncology
  • Support/contribute to protocol development to ensure appropriateness of trial design, sample size, and propose the use of meaningful and efficient statistical methodologies
  • Lead development of statistical analysis plans, data presentation plans, clinical development plans, biometrics related submission activities, and post-submission strategies/responses
  • Review the accuracy of clinical data, perform statistical analysis, interpret study results, and collaborate with clinical team and other team members to produce interim reports, final reports, and publications
  • Write/review sections of meeting packages and assist in the development and review of other documents required for regulatory submissions and other regulatory processes
  • Review vendor data transfer specifications and ADaM programming specifications
  • Lead assessment and introduction of novel statistical methodologies to implement solutions
  • Represent biostatistics function or biometrics department in cross function teams
  • Work with department leader to develop and implement department policies, standards and procedures
  • Collaborate with clinical operations, data management and CRO to develop and implement CRFs, database design, and the overall data quality plan
  • Evaluate and manage CROs and other vendors, including scope-of-work, timelines, deliverables and budgets
  • Provide strategic statistical and regulatory guidance to anticipate challenges, mitigate risk, and ensure project success
  • Attend meetings with FDA or other health authorities to ensure ongoing agreement on project development
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:

  • PhD and a minimum of 8+ years of experience or Masters (MS) and a minimum of 11+ years of experience in statistics or biostatistics or related disciplines with clinical trials, pharmaceutical/biotech industry, or healthcare experience
  • Experience in supporting oncology phase II/III clinical studies
  • Experience in organizing and driving regulatory submissions (e.g. NDA, sNDA, BLA)
  • In-depth knowledge of CDISC standards
  • Technical expertise and knowledge of experimental design and analyses using SAS, R, or EAST, and etc.
  • Excellent written and verbal communication skills
  • Good working knowledge of ICH, FDA and GCP regulations and guidelines

Apply