... 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.
... 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.
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 ...
Hybrid as needed 2 days/week in Seattle, WA Ascendion is hiring an ADaM/TLF & FDA Submission Expert ... ADaM dataset structure Job details Job ID 332875 Role Clinical Statistical Programmer Location ...
Hybrid as needed 2 days/week in Seattle, WA Ascendion is hiring an ADaM/TLF & FDA Submission Expert ... ADaM dataset structure Job details Job ID 332875 Role Clinical Statistical Programmer Location ...
Serve as primary or lead programmer for agency reporting deliverables such as DSUR/Annual Report ... and 2+ years * At least three years of experience serving in a supervisory or lead capacity
Serve as primary or lead programmer for agency reporting deliverables such as DSUR/Annual Report ... and 2+ years * At least three years of experience serving in a supervisory or lead capacity
* 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 ...
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 ...
Director/Principal, Statistical Programming
New York, NY · On-site
$233K - $244K/yr
... programmer on CNS clinical trials (schizophrenia, bipolar depression, MDD), including Phase 2 and ... Lead statistical programming activities for IND/NDA submissions, including Integrated Summary of ...
Director/Principal, Statistical Programming
New York, NY · On-site
$233K - $244K/yr
... programmer on CNS clinical trials (schizophrenia, bipolar depression, MDD), including Phase 2 and ... Lead statistical programming activities for IND/NDA submissions, including Integrated Summary of ...
Lead Statistical Analyst
Cincinnati, OH · On-site
$130K - $150K/yr
... 2. Leads a team of statistical programmers and manages the resource planning for assigned staff. 3. Ensures timely deliverables, that all quality processes are followed and consistency within the ...
Lead Statistical Analyst
Cincinnati, OH · On-site
$130K - $150K/yr
... 2. Leads a team of statistical programmers and manages the resource planning for assigned staff. 3. Ensures timely deliverables, that all quality processes are followed and consistency within the ...
Director/Principal, Statistical Programming
New York, NY · Remote
$233K - $244K/yr
... programmer on CNS clinical trials (schizophrenia, bipolar depression, MDD), including Phase 2 and ... Lead statistical programming activities for IND/NDA submissions, including Integrated Summary of ...
Quick apply
Director/Principal, Statistical Programming
New York, NY · Remote
$233K - $244K/yr
... programmer on CNS clinical trials (schizophrenia, bipolar depression, MDD), including Phase 2 and ... Lead statistical programming activities for IND/NDA submissions, including Integrated Summary of ...
Posted 2 Days Agojob requisition id: JR\_000770Madrigal is a biopharmaceutical company focused on ... The Principal / Associate Director Statistical Programmer is an individual contributor responsible ...
Posted 2 Days Agojob requisition id: JR\_000770Madrigal is a biopharmaceutical company focused on ... The Principal / Associate Director Statistical Programmer is an individual contributor responsible ...
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 ...
Senior Manager, Statistical Programming
San Francisco, CA · On-site
$169K - $219K/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 ...
Senior Manager, Statistical Programming
San Francisco, CA · On-site
$169K - $219K/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 ...
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 ...
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 ...
Chapman University School of Pharmacy is seeking an Assistant Statistical Research Programmer to ... two of the mentioned languages. Preferred : • Master's Degree in related field. • A good ...
Chapman University School of Pharmacy is seeking an Assistant Statistical Research Programmer to ... two of the mentioned languages. Preferred : • Master's Degree in related field. • A good ...
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 ...
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 ...
Senior Manager, Statistical Programming - Oncology Early Development
South San Francisco, CA · On-site
Minimum of 2 years experience leading a team of statistical programmers. * In‑depth understanding of SAS programming concepts and techniques related to drug development. * In‑depth understanding ...
Senior Manager, Statistical Programming - Oncology Early Development
South San Francisco, CA · On-site
Minimum of 2 years experience leading a team of statistical programmers. * In‑depth understanding of SAS programming concepts and techniques related to drug development. * In‑depth understanding ...
Implement Statistical Analysis Plans (SAP) and SPP to create ADaM data specifications. 2. Program and validate ADaM and statistical analyses using programming languages (e.g., SAS, R), ensuring ...
Quick apply
Implement Statistical Analysis Plans (SAP) and SPP to create ADaM data specifications. 2. Program and validate ADaM and statistical analyses using programming languages (e.g., SAS, R), ensuring ...
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
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Sr. Principal Analyst, Statistical Programming
San Diego, CA • On-site
Other
Medical, Dental, Vision, Retirement, PTO
Posted 5 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, visit neurocrine.com , and follow the company on LinkedIn , X and Facebook . ( *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
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Neurocrine Biosciences is an EEO/Disability/Vets employer.
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.