Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables. * Provide statistical and validation support for statistical ...

60 Labcorp Principal Statistical Programmer Jobs Hiring Near You
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables. * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables. * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables. * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables. * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables. * Provide statistical and validation support for statistical ...
Principal Statistical Programmer, PKPD
Durham, NC · On-site
$98.20K - $273.20K/yr
PK parameter pooling Experience * 8+ years of statistical programming experience in the pharmaceutical or CRO environment. * Demonstrated experience as a Lead Programmer or technical lead. * Prior ...
Principal Statistical Programmer, PKPD
Durham, NC · On-site
$98.20K - $273.20K/yr
PK parameter pooling Experience * 8+ years of statistical programming experience in the pharmaceutical or CRO environment. * Demonstrated experience as a Lead Programmer or technical lead. * Prior ...
Principal Statistical Programmer, PKPD
$98.20K - $273.20K/yr
PK parameter pooling Experience * 8+ years of statistical programming experience in the pharmaceutical or CRO environment. * Demonstrated experience as a Lead Programmer or technical lead. * Prior ...
Principal Statistical Programmer, PKPD
$98.20K - $273.20K/yr
PK parameter pooling Experience * 8+ years of statistical programming experience in the pharmaceutical or CRO environment. * Demonstrated experience as a Lead Programmer or technical lead. * Prior ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables * Provide statistical and validation support for statistical ...
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables * Provide statistical and validation support for statistical ...
The Principal Statistical Programmer is responsible for providing leadership and hands-on support in the development and maintenance of the CSL statistical programming capabilities which is required ...
The Principal Statistical Programmer is responsible for providing leadership and hands-on support in the development and maintenance of the CSL statistical programming capabilities which is required ...
The Principal Statistical Analyst will be responsible for supporting and/or leading the statistical programming activities for clinical trial data collection, analysis, reporting, visualization on ...
The Principal Statistical Analyst will be responsible for supporting and/or leading the statistical programming activities for clinical trial data collection, analysis, reporting, visualization on ...
The Principal Statistical Analyst will be responsible for supporting and/or leading the statistical programming activities for clinical trial data collection, analysis, reporting, visualization on ...
The Principal Statistical Analyst will be responsible for supporting and/or leading the statistical programming activities for clinical trial data collection, analysis, reporting, visualization on ...
Statistical Programmer
Denver, CO · On-site +1
Direct message the job poster from Digital Prospectors Principal Recruiter at Digital Prospectors Position: Statistical Programmer Length: 10+ months *W2 Candidates Only, No C2C Our client is seeking ...
Statistical Programmer
Denver, CO · On-site +1
Direct message the job poster from Digital Prospectors Principal Recruiter at Digital Prospectors Position: Statistical Programmer Length: 10+ months *W2 Candidates Only, No C2C Our client is seeking ...
Sr Principal Analyst, Statistical Programming
Cambridge, MA · On-site
$141K - $188K/yr
About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data ...
Sr Principal Analyst, Statistical Programming
Cambridge, MA · On-site
$141K - $188K/yr
About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data ...
NC · On-site
$134K - $179K/yr
About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data ...
Sr Principal Analyst, Statistical Programming
Cambridge, MA · On-site
$141K - $188K/yr
About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data ...
Sr Principal Analyst, Statistical Programming
Cambridge, MA · On-site
$141K - $188K/yr
About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data ...
Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of ...
Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of ...
Principal Programmer, Statistical Programming
San Diego, CA · On-site
$154.16K - $195K/yr
The Principal Programmer, Statistical Programming, will be responsible for leading programming activities for multiple studies to support clinical development, medical affairs, drug safety, CSR and ...
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Principal Programmer, Statistical Programming
San Diego, CA · On-site
$154.16K - $195K/yr
The Principal Programmer, Statistical Programming, will be responsible for leading programming activities for multiple studies to support clinical development, medical affairs, drug safety, CSR and ...
Sr. Principal Analyst, Statistical Programming
San Francisco, CA · On-site
$141K - $188K/yr
About This Role The Senior Principal Analyst, Statistical Programming reporting to Statistical Programming Manager, West Coast Hub, Biogen. He/She will lead and oversee statistical programming ...
Sr. Principal Analyst, Statistical Programming
San Francisco, CA · On-site
$141K - $188K/yr
About This Role The Senior Principal Analyst, Statistical Programming reporting to Statistical Programming Manager, West Coast Hub, Biogen. He/She will lead and oversee statistical programming ...
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early ...
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early ...
Sr. Principal Analyst, Statistical Programming
$141K - $188K/yr
About This Role The Senior Principal Analyst, Statistical Programming reporting to Statistical Programming Manager, West Coast Hub, Biogen. He/She will lead and oversee statistical programming ...
Sr. Principal Analyst, Statistical Programming
$141K - $188K/yr
About This Role The Senior Principal Analyst, Statistical Programming reporting to Statistical Programming Manager, West Coast Hub, Biogen. He/She will lead and oversee statistical programming ...
Senior Principal Statistical Programmer - Advanced Quantitative Sciences
East Hanover, NJ · On-site +1
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Principal Statistical Programmer - Advanced Quantitative Sciences
East Hanover, NJ · On-site +1
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Labcorp Jobs Information
What is a Principal Statistical Programmer job?
What are the key skills and qualifications needed to thrive in the Principal Statistical Programmer position, and why are they important?
What are the typical daily responsibilities of a Principal Statistical Programmer in a clinical research setting?
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Other
Posted 23 days ago
Job description
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
Responsibilities:
- Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
- Review CRF, database design, and edit check specs.
- Review study quality surveillance plan and monitor study conduct.
- Prepare and/or review SAP, TFL shells and specifications for variable derivation.
- Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables.
- Provide statistical and validation support for statistical analysis, analysis datasets and TFL.
- Review study report, manuscripts and other documents related to statistics.
- Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents.
- Perform other ad-hoc statistical activities as needed.
- Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming.
- Participates in monitoring CRO activities and reviewing CRO deliverables Other duties as assigned.
- Ph.D. or MS in Statistics or Biostatistics.
- Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience.
- Excellent knowledge of SAS computer package.
- Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines.
- Excellent organizational skills, time management, and ability to meet established deadlines.
- Excellent communication and interpersonal skills to effectively interface with others.
- Ability to work independently and problem-solve.
- Ability to provide leadership for the CRO statisticians and statistical programmers.
About Katalyst Healthcares & Life Sciences
Sourced by ZipRecruiter
Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
South Plainfield, NJ, US