29 days old

SVP Statistical and Programming Leader

Kelly Services
South San Francisco, CA 94080
  • Jobs Rated
Kelly Scientific is seeking an **SVP level leader** who will be responsible for managing statisticians, programmers, and consultants to support all statistical and programming needs for programs from pre-IND through Commercialization. As a member of the Clinical Development, Operations, and Medical Affairs team, the ideal candidate will play a key role in strategic planning for all clinical programs and across all R&D functions.

**This will be a full-time remote position** .


+ Provide strategic and statistical expertise in design of clinical development plans, clinical study protocols, analysis, and clinical study reports.

+ Functional Representative in key internal facing senior meetings such as program teams, clinical development, operations, and regulatory affairs leadership team, portfolio steering team and management team, as well as more external facing meetings such as Board of Directors.

+ Summarize and present statistical strategies and/or key study results to internal governance bodies, external collaborators including business partners and regulatory agencies.

+ Plan and oversee deliverables and timeline of study readouts including regular data reviews, predefined interim analysis, and final analysis to support decision making.

+ Work closely with clinical development, clinical operations, pharmacovigilance, clinical pharmacology, translational science, and medical writing to support clinical study planning and execution.

+ Manage an existing team of statisticians and statistical programmers and support and foster their professional development needs and build the team as company progresses.

+ Represent Biostatistics function in the program team and contribute to cross-functional decision making on study design, endpoint selection, data collection, and analysis strategies, ensuring alignment with study objectives.

+ Perform sample size calculation for continuous, dichotomous, and time to event endpoints in various study design.

+ Perform simulation studies to explore the statistical operating characteristics in study design phase including innovative/adaptive designs.

+ Proactively identify and anticipate technical or data related issues arising in the design, conduct or analysis of clinical trials or other scientific research, and approve and implement alternative analysis strategies or other recommendations to address these issues.

+ Evaluate performance of patient enrichment biomarkers including metrics for AUC, PPV, NPV and determination of assay thresholds for use in prospective trials.

+ Write the statistical section in clinical protocols.

+ Develop statistical analysis plans, coordinate, and perform data analysis and validation as necessary, and provide data interpretation.

+ Develop exploratory statistical analysis plans for predictive and pharmacodynamic biomarkers and help develop companion diagnostics strategies for the program.

+ Interpret study results and write (or at least QC and review) statistical summary reports of study results.

+ Perform statistical analyses to support publications in medical conferences

+ Collaborate with data management team to support QC of CRO activities to include UAT, Query management, Data review, DM documentation such as DMP, DVS, edit checks, coding, lock process.

+ Support development of eCRFs and be responsible for specs for IVRS, SDTM, and ADaM.

+ Contribute to the implementation, maintenance, and evolution of the systems and processes involved in the collection, review, and analysis of clinical and translational data.

+ Responsible for statistical programming activities including the development of standard statistical documents such as TLFs, Programming specs (e.g., SDTM and ADaM), SAS macros, and SOPs.

+ Develop proper resources and process regarding hardware, software, SOP and work instructions to provide effective support to clinical studies and ascertain needs for potential program development of novel statistical methodology.


+ PhD or equivalent in Statistics or Biostatistics required.

+ 12+ years of experience in pharmaceutical development and applied statistics/statistical consulting required, experience in Central Nervous System (CNS) a plus.

+ 7+ years of management experience leading biostatistics and programming groups.

+ Experience with drug development in biologics, targeted therapies, and companion diagnostics preferred.

+ Knowledge of FDA, EMA, and ICH guidance for drug development pertaining to statistics.

+ Experience with the relevant regulatory requirements for data management and supporting SOPs.

+ Experience in use of commercial clinical data management systems/EDC products (e.g., RAVE, Inform, TrialMaster, etc.).

+ Experience with regulatory submissions including BLAs and previous experience in dealing with Health authorities such as discussions/negotiations in filing strategies.

+ Familiar with SDTM, ADaM, eSUB, and CDISC requirements for regulatory submissions.


+ Demonstrated ability to work independently, handle multiple priorities within timelines, and collaborate with other functions to resolve issues and improve efficiency.

+ Excellent inter-personal skills in management, collaboration, and communication to managers, colleagues, team members, CROs, external statistical / medical experts, and external collaborators.

+ Enthusiastic, passionate about bringing important new therapies to patients with cancer, and willing to roll up their sleeves to do whatever it takes while building the right team of outstanding statistics and data management professionals.

+ Effective communication skills and able to explain complex statistical approaches to non-statisticians.

Equal Opportunity Employer and will not discriminate against any applicant for employment based on race, age, religion, sex, veterans, and individuals with disabilities, sexual orientation, or gender identity.


**You should know:** Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.

**Why Kelly** **** **?**

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

**About Kelly** ****

At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. (


Jobs Rated Reports for Statistician

Posted: 2022-05-27 Expires: 2022-06-27

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

SVP Statistical and Programming Leader

Kelly Services
South San Francisco, CA 94080

Join us to start saving your Favorite Jobs!

Sign In Create Account
2nd2019 - Statistician
Overall Rating: 2/199
Median Salary: $84,760

Work Environment
Very Good
Very Low
Very Good
Powered ByCareerCast