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 ...
... 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.
RWE Biostatistician, RWE Statistical Programmer (Remote)
Basking Ridge, NJ · Remote
$95K - $205K/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 - $205K/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 ...
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 ...
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 ...
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 ...
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
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 ...
May function as lead programmer to produce or validate tables, listings, figures and analysis ... At least 2 years management experience. * Knowledge of clinical trials and experience in using SAS ...
May function as lead programmer to produce or validate tables, listings, figures and analysis ... At least 2 years management experience. * Knowledge of clinical trials and experience in using SAS ...
... 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.
* 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 ...
Associate Director, Clinical and Statistical Programming
$185.10K - $228.70K/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
$185.10K - $228.70K/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 ...
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 ...
OR · On-site
$153.94K - $199.21K/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
$153.94K - $199.21K/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 ...
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
$154.16K - $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
$154.16K - $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
R&D Programmer II
Parsippany, NJ · Remote
Up to 2 year assignment Shift Schedule: Regular 40-hour work week (morning shift) Position Summary ... Proactively communicates issues impacting programming deliverables with Statistics or Data ...
R&D Programmer II
Parsippany, NJ · Remote
Up to 2 year assignment Shift Schedule: Regular 40-hour work week (morning shift) Position Summary ... Proactively communicates issues impacting programming deliverables with Statistics or Data ...
Statistical Programmer Two 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
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$84.5K
$147.3K
$249K
How much do statistical programmer two jobs pay per year?
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 4 days ago
Job description
At Pacira, innovation meets purpose.
Pacira BioSciences, Inc. is a pioneer in non-opioid pain management and regenerative health solutions. Today, we're building on that legacy with next-generation innovations for chronic, postsurgical, and musculoskeletal pain. Our culture is built on collaboration, innovation, and a shared commitment to helping patients recover faster. We are redefining what's possible in pain management-and we can't do it without talented people like you.
Why Join Us?
At Pacira, every career is more than a job. Our mission drives us, and every day, we challenge ourselves to achieve the extraordinary. Integrity is at the core of who we are. We value diverse perspectives and the collective strength of a unified team. Join the team in making better possible for patients everywhere.
Summary:
The Manager, Statistical Programming will work in Statistical Programming group to manage and support Statistical Programming deliverables for clinical studies.
Responsibilities
Essential Duties & Responsibilities:
- Technical lead and project manager for multiple studies managing all aspects of study deliverables related to statistical and clinical programming as needed
- Represent the statistical programming team at Study Management Team and Clinical Development meetings to address deliverables and timelines
- Address resourcing to adequately staff projects as needed
- Assist in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans and other clinical documents
- Write, test, and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications as needed
- Understand and execute department-, product- and study-level macros and utilities. Write, test, and validate product- and study-level macros and utilities
- Be a technical resource for programming group to provide advice on complex programming tasks and/or standards.
- Contribute to the development review of Statistical Programming policies, standard operating procedures, and other controlled documents
- Interface with outsourcing partners and vendor
Supervisory Responsibilities:
No supervisory responsibilities
Interaction:
Interact and communicate with R&D Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Directors to address programming related study deliverables.
Qualifications
Education and Experience:
- Bachelor's degree or above in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject, or equivalent related experience required.
- Minimum 2+ years' clinical research and development programming experience using SAS or advanced degree required.
Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Knowledge, Skills, and Abilities:
- Knowledge of SDTM and ADaM standards, able to write CDISC standard dataset specifications and follow specifications to create SDTM and ADaM datasets (as needed)
- Computer programming using SAS essential, and experience with R and Python desirable
- Fundamentals of project planning and management
- Drug development process
- Excellent verbal and written communication skills
- Ability to effectively collaborate in a dynamic environment
- Expert level SAS programmer with experience in delivering on complex programming assignments and analysis
- Expert level knowledge and extensive hands-on experience of CDISC methodologies
- Experience leading or working with centralized teams for Statistical Programming
- Experience in FDA/EMEA/CFDA trial and regulatory submissions
- Experience with the drug development process (pre-, early, late and/or observational) in related industries or academic research
Physical Demands:
While performing the duties of this job, the employee is regularly required to sit, talk, move between spaces, reach with hands and arms and stoop. Close vision and the need to focus on computer screen, use of hands, fingers and wrist to type on keyboard and manipulate mouse.
Work Environment:
The work will be in a typical office environment (cubicles, offices, conference rooms, etc.) with heavy computer use.
Benefits
- Medical, Prescription, Dental, Vision Coverage
- Flexible Spending Account & Health Savings Account with Company match
- Employee Assistance Program
- Mental Health Resources
- Disability Coverage
- Life insurance
- Critical Illness and Accident Insurance
- Legal and Identity Theft Protection
- Pet Insurance
- Fertility and Maternity Assistance
- 401(k) with company match
- Flexible Time Off (FTO) and 11 paid holidays
- Paid Parental Leave
Pay Transparency
The base pay range for this role is $103,000 to 140,000 per year. The range is what we reasonably expect to pay for this role. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications. Depending on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered.
EEO Statement
EEO Statement: Pacira is proud to be an Equal Opportunity Employer and does not discriminate against applicants because of race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age (40 or older), veteran status, disability or genetic information, or any other characteristic protected under applicable federal, state, or local law. At Pacira we are committed to intentionally cultivating a culture of inclusion where all feel welcomed and valued for their background, perspectives, and experiences. We hold one another accountable to promote trust and transparency in support of our communities and collective purpose.
Agency Disclaimer: Pacira Biosciences, Inc. (Hereafter, Pacira) does not accept unsolicited resumes from recruiters or employment agencies in response to the Pacira Careers page or a Pacira social media post. Pacira will not consider or agree to payment of any referral compensation or recruiter fee relating to unsolicited resumes. Pacira explicitly reserves the right to hire said candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Pacira.
About Pacira Pharmaceuticals
Sourced by ZipRecruiter
Industry
Manufacturing
Company size
501 - 1,000 Employees
Headquarters location
San Diego, CA, US
Year founded
1989