Neurocrine Biosciences · 22 hours ago
Sr. Analyst, Stats Programming
US CA San Diego
Full-time
Onsite
Mid, Senior Level
$111K/yr - $151K/yr
4+ years expNeurocrine Biosciences is a leading neuroscience-focused biopharmaceutical company dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological disorders. The role involves designing, developing, testing, and maintaining SAS programs for clinical data evaluation while providing technical expertise to programming standards and procedures.
BiotechnologyHealthcarePharmaceuticalHealth Care
Responsibilities
Serves as the primary project team representative, delegating work as appropriate
Generates SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data
Reviews output across programs to ensure consistency
Reviews maintains and approves study documents per standard procedures
Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures
Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting
Participates in the development and/or maintenance of departmental procedures and standards
Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures
Implements data management plans designed to meet project and protocol deadlines
Acts as a liaison between clinical management, subcommittees and project teams as needed
May train and mentor new programmers
Performs other duties as assigned
Qualification
Required
BS/BA degree in computer science, mathematics, statistics, or related discipline AND 4+ years experience in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph). In addition, must have at least three years of experience serving in a supervisory or lead capacity. Experience managing projects OR
Master's degree in computer science, mathematics, statistics, or related discipline AND 2+ years of similar experience noted above OR
PhD in computer science, mathematics, statistics, or related discipline AND similar experience as noted above
Understands key business drivers and uses this understanding to accomplish work
Has strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas
Proficient with tools and processes that support work conducted by functional area
Ability to work as part of a team; may train lower levels
Excellent computer skills
Strong communications, problem-solving, analytical thinking skills
Detail oriented yet can see broader picture for department
Ability to meet multiple deadlines, with a high degree of accuracy and efficiency
Strong project management skills
Strong interpersonal skills to effectively work in a team environment
Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines
Proficiency with Word, Excel, and PowerPoint is required as is the ability to communicate effectively both verbally and in writing
Demonstrates strong knowledge with industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
Strong programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar
Strong knowledge of SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Strong knowledge of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems
Strong understanding of relational databases and experience working with complex data systems
Benefits
Annual bonus with a target of 20% of the earned base salary
Eligibility to participate in our equity based long term incentive program
Retirement savings plan (with company match)
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans
Company
Neurocrine Biosciences
Neurocrine Biosciences engages in the discovery and development of drugs for the treatment of neurological and endocrine-related diseases.
1001-5000 employees
H1B Sponsorship
Neurocrine Biosciences has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (16)
2024 (9)
2023 (8)
2022 (2)
2021 (5)
2020 (6)
Funding
Current Stage
Public CompanyTotal Funding
$260MKey Investors
Venrock
2015-02-19Post Ipo Equity· $250M
2009-12-17Post Ipo Equity· $10M
1996-05-31IPO
Leadership Team
Matt Abernethy
Chief Financial Officer
D
Dimitri Grigoriadis
VP, Research
Recent News
2026-02-11
Company data provided by crunchbase