Tallo logoTallo logo

Associate Director, Biostatistics and Statistical Programming

Job

OREGON EMPLOYMENT DEPARTMENT

Remote

Part-Time

Posted 4 weeks ago (Updated 3 weeks ago) • Actively hiring

Expires 5/28/2026

Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
84
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Job Listing ID:
4472773
Job Title:
Associate Director, Biostatistics and Statistical Programming Application Deadline:
Open Until Filled
Job Location:
Salem
Date Posted:
04/14/2026
Hours Worked Per Week:
Not Provided Shift:
Not Provided Duration of Job:
Either Full or Part Time, more than 6 months You may contact this employer directly. (Obtain the contact information to print or add to your jobs.)
Job Summary:
Overview The Associate Director, Biostatistics and Statistical Programming will drive biostatistical activities, performed primarily by vendors, in support of project timelines and budgets related to drug product development at Xeris. The individual will contribute to study design, protocol development, case report form development, clinical study reports, and exhibits for other reports and presentations. Responsibilities Conducts basic statistical analysis of study datawith minimal supervision according to a statistical analysis planto generate results and insights used to support study findings. Applies moderately advanced statistical methods, which may include simulation models and other statistical programming as needed, with guidance. Generates sample size and power calculations and randomizations. Oversees the review of statistical documents and operational activities outsourced to CROs ensuring adherence to cost, timeline, and data quality requirements to ensure that the analysis plans use the most appropriate statistical methods and that the data displays such as tables/figures/listings are accurate and complete. Programs or independently validates key study results to support interpretation of data. Provides statistical programming support to other clinical studies or regulatory submissions where another biostatistician is assigned as the sponsor lead. Works closely with Data Management by providing input to data management-related documents and assisting with data review and cleaning activities, as needed. Ensures compliance of data packages to regulatory requirements and CDISC and industry standards. Assists in the development of abstracts, manuscripts, presentations for scientific congresses. Closely collaborates and participates in knowledge sharing with other team members including non-statisticiansto assist with interpretation and understanding of results. Qualifications MS/MPH degree in biostatistics, statistics, or epidemiology A minimum of six years of clinical trial experience as a statistician and/or statistical programmer in the pharmaceutical, biotech, or CRO industry Experience in Phases I-III of the clinical drug development process Knowledge and basic understanding of statistical concepts and techniques commonly applied to the analysis of data from clinical trials and the ability to tackle from basic to moderately complex statistical or data issues Basic understanding of real-world data and observational studies. SAS programming experience required, R experience is a plus Working knowledge of CDISC standards Prior use and implementation of sample size and power calculation software (e.g., nQuery and PASS) preferred Working knowledge of EDC systems
Competencies:
Attention to Detail, Organizational skills, Adaptability, Multi-Tasking, Strong Written & Verbal Communication skills,
Teamwork & Collaboration, Critical Thinking, Problem Solving, Presentation Skills Working Conditions:
Preference will be given to qualified candidates in the Chicagoland area. If based in Chicago, the position is hybrid and a minimum of three days per week on-site at Xeris' Chicago office is required. On-site requirement may change at management's discretion. Position may require periodic evening and weekend work, as necessary to fulfill obligations. Periodic overnight travel. The level of the position will be determined based on the selected candidate's qualifications and experience. #
LI-REMOTE
As an equal employment opportunity and affirmative action employer, Xeris Pharm...
Job Classification:
Data Scientists Access our statewide or regional occupation report for more information about wages, employment outlooks, skills, training programs, related occupations, and more. Compensation
Salary:
Not Provided Job Requirements
Experience Required:
 See Job Summary
Education Required:
None
Minimum Age:
N/A Gender:
N/A

Similar remote jobs

Similar jobs in Salem, MA

Similar jobs in Massachusetts