... programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity.
... programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity.
The Manager, Statistical Programming will work in Statistical Programming group to manage and ... Minimum 2+ years' clinical research and development programming experience using SAS or advanced ...
The Manager, Statistical Programming will work in Statistical Programming group to manage and ... Minimum 2+ years' clinical research and development programming experience using SAS or advanced ...
RWE Biostatistician, RWE Statistical Programmer (Remote)
Basking Ridge, NJ · Remote
$95K - $204K/yr
MarketScan); 2) US medical record databases (e.g. GE Healthcare); 3) US government public use ... Conduct observational data analysis, include data management, statistical programming ...
Quick apply
RWE Biostatistician, RWE Statistical Programmer (Remote)
Basking Ridge, NJ · Remote
$95K - $204K/yr
MarketScan); 2) US medical record databases (e.g. GE Healthcare); 3) US government public use ... Conduct observational data analysis, include data management, statistical programming ...
Min 2-3 years of programming experience in HARP, the GSK programming environment is required. At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical ...
Min 2-3 years of programming experience in HARP, the GSK programming environment is required. At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical ...
Statistical Programming Associate Director
Marlborough, MA · On-site
$168K - $210K/yr
Minimum 8 years or equivalent Pharmaceutical/Biotech programming experience with two years of ... Strong SAS programming and Statistical background along with experience with SAS Base, SAS/Macros ...
Statistical Programming Associate Director
Marlborough, MA · On-site
$168K - $210K/yr
Minimum 8 years or equivalent Pharmaceutical/Biotech programming experience with two years of ... Strong SAS programming and Statistical background along with experience with SAS Base, SAS/Macros ...
Statistical Programming Associate Director
$168K - $210K/yr
Minimum 8 years or equivalent Pharmaceutical/Biotech programming experience with two years of ... Strong SAS programming and Statistical background along with experience with SAS Base, SAS/Macros ...
Statistical Programming Associate Director
$168K - $210K/yr
Minimum 8 years or equivalent Pharmaceutical/Biotech programming experience with two years of ... Strong SAS programming and Statistical background along with experience with SAS Base, SAS/Macros ...
Sr. Manager, Statistical Programming
Boston, MA · On-site +1
$151K - $172K/yr
Ensure the statistical programming processes and deliverables are aligned with regulatory ... Some domestic and international travel required (2-3 times per year) * On-site in Boston ...
New
Sr. Manager, Statistical Programming
Boston, MA · On-site +1
$151K - $172K/yr
Ensure the statistical programming processes and deliverables are aligned with regulatory ... Some domestic and international travel required (2-3 times per year) * On-site in Boston ...
New
* Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or ...
* Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or ...
... programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity.
... programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity.
Associate Director, Clinical and Statistical Programming
Seattle, WA · On-site
$185K - $228K/yr
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days ... Lead statistical programming activities for clinical trials and ensure the timely delivery of high ...
Associate Director, Clinical and Statistical Programming
Seattle, WA · On-site
$185K - $228K/yr
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days ... Lead statistical programming activities for clinical trials and ensure the timely delivery of high ...
Junior Statistical Programmer
East Brunswick, NJ · On-site +1
Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or ...
Junior Statistical Programmer
East Brunswick, NJ · On-site +1
Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or ...
OR · On-site
$153K - $199K/yr
Statistical programmers work collaboratively with internal colleagues and external vendors to ... PhD degree in Biostatistics/Computer Sciences or equivalent 2+ years of experience in pharma ...
OR · On-site
$153K - $199K/yr
Statistical programmers work collaboratively with internal colleagues and external vendors to ... PhD degree in Biostatistics/Computer Sciences or equivalent 2+ years of experience in pharma ...
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days ... Lead statistical programming activities for clinical trials and ensure the timely delivery of high ...
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days ... Lead statistical programming activities for clinical trials and ensure the timely delivery of high ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Experience leading large and/or complex statistical programming projects for Phase 2 and 3 clinical trials, including coordinating the activities of a programming team. * US and/or worldwide drug ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Experience leading large and/or complex statistical programming projects for Phase 2 and 3 clinical trials, including coordinating the activities of a programming team. * US and/or worldwide drug ...
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days ... Lead statistical programming activities for clinical trials and ensure the timely delivery of high ...
Quick apply
This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days ... Lead statistical programming activities for clinical trials and ensure the timely delivery of high ...
Principal Programmer, Statistical Programming
San Diego, CA · On-site
$154K - $195K/yr
The Principal Programmer, Statistical Programming, will be responsible for leading programming ... Minimum 2 years of experience in developing software in a clinical trial environment using SQL, SAS ...
Quick apply
Principal Programmer, Statistical Programming
San Diego, CA · On-site
$154K - $195K/yr
The Principal Programmer, Statistical Programming, will be responsible for leading programming ... Minimum 2 years of experience in developing software in a clinical trial environment using SQL, SAS ...
A minimum of one year of experience in statistical programming with Python, SAS, or R, with a preference for candidates proficient in at least two of the mentioned languages. Desired Qualifications
A minimum of one year of experience in statistical programming with Python, SAS, or R, with a preference for candidates proficient in at least two of the mentioned languages. Desired Qualifications
Basic Qualifications: • Doctorate degree OR • Master's degree and 2 years of statistical programming experience OR • Bachelor's degree and 4 years of statistical programming experience OR • ...
Basic Qualifications: • Doctorate degree OR • Master's degree and 2 years of statistical programming experience OR • Bachelor's degree and 4 years of statistical programming experience OR • ...
Computer Programmer II
Hyattsville, MD · On-site
The Computer Programmer II provides mid-level software development and maintenance support for the National Vital Statistics System (NVSS), National Death Index (NDI), and related CDC/NCHS DVS ...
Computer Programmer II
Hyattsville, MD · On-site
The Computer Programmer II provides mid-level software development and maintenance support for the National Vital Statistics System (NVSS), National Death Index (NDI), and related CDC/NCHS DVS ...
Statistical Programmer 2 information
See salary details
$84.5K - $99.5K
3% of jobs
$99.5K - $114.4K
10% of jobs
$124.5K is the 25th percentile. Wages below this are outliers.
$114.4K - $129.4K
18% of jobs
The median wage is $144.3K / yr.
$129.4K - $144.3K
19% of jobs
$157.3K is the 75th percentile. Wages above this are outliers.
$144.3K - $159.3K
29% of jobs
$159.3K - $174.2K
10% of jobs
$174.2K - $189.2K
12% of jobs
$189.2K - $204.1K
0% of jobs
$204.1K - $219.1K
0% of jobs
$219.1K - $234K
0% of jobs
$234K - $249K
0% of jobs
$84.5K
$147.3K
$249K
How much do statistical programmer 2 jobs pay per year?
What are the key skills and qualifications needed to thrive as a Statistical Programmer 2, and why are they important?
How does a Statistical Programmer 2 typically collaborate with biostatisticians and clinical teams during a clinical trial project?
What are Statistical Programmer 2s?

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 22 days ago
Job description
At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.
What We Do:Neurocrine Biosciencesis a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visitneurocrine.com, and follow the company onLinkedIn,XandFacebook. (*in collaboration with AbbVie)
About the Role:Leads major statistical programming efforts for clinical program area of responsibility. Develops and recommends system capabilities roadmap for in-house development and external vendor selection process. Acts as a system expert in designing, developing, testing, maintaining, validating, and documenting SAS programs to evaluate clinical data and meet the project requirements for SAS statistical programming efforts. Provides expert-level technical advice for all aspects of the program development process, tools and software, standards and procedures._
Your Contributions (include, but are not limited to):Provides expert technical leadership across multiple functions serving as the key representative for Biometrics
Contributes to the development of Biometrics functional strategy and serves as system expert for Statistical Programming efforts
Leads and mentors a team of statistical programmers to support the analysis and reporting of data from clinical and nonclinical studies for all corporate development programs
Leads end-to-end statistical programming work-streams on multidisciplinary program teams company-wide
Provides technical direction in the development and implementation of programming standards and conventions, building statistical programming infrastructure
Provides workforce planning recommendations based on project workloads in order to ensure appropriate programming resources are available to complete tasks in a timely manner
Manages vendor selection processes and validates vendor programming activities such as CDISC implementation, analysis reporting, and programming conventions
Supports creation and validation of e-submission requirements (i.e. annotated CRF, datasets files, define documents)
Serves as primary/lead programmer for agency reporting deliverables such as DSUR/Annual Report and IB updates
Performs the function of lead and/or quality control statistical programmer on projects as needed
Performs other duties as assigned
BS/BA degree in computer science, mathematics, statistics, or related discipline AND 8+ years in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity. Experience managing large projects and external vendors. OR
Master's degree in computer science, mathematics, statistics, or related discipline AND 6+ years similar experience noted above OR
PhD degree in computer science, mathematics, statistics, or related discipline AND 4+ years similar experience noted above
Anticipates business and industry issues; recommends relevant process / technical / service improvements
Demonstrates broad expertise or unique knowledge
Considered an expert within the company and may have external presence in area of expertise
Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency of team
Ability to work as part of and lead multiple teams
Good leadership, mentoring skills and abilities typically leads lower levels and/or indirect teams
Excellent computer skills
Excellent communications, problem-solving, analytical thinking skills
Sees broader picture and longer-term impact on division/company
Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
Excellent project management, strong project leadership skills
Expert knowledge of the following:
Developing and implementing statistical programming SOPs and processes in a clinical environment
Relational databases and complex data systems.
Industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
Programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar
SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Knowledge of all aspects of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems
Proven experience in multi-discipline, cross-functional project management in a clinical, highly regulated environment
Track record of success with effectively organizing and managing multiple assignments with challenging timelines across multiple personnel
#LI_SA1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
_
The annual base salary we reasonably expect to pay is $156,900.00-$214,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.About Neurocrine Biosciences
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
1,001 - 5,000 Employees
Headquarters location
San Diego, CA, US
Year founded
1992