King Of Prussia, PA · Remote
$100K - $160K/yr
The RWE Statistician is involved in planning, conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database ...
Quick apply
King Of Prussia, PA · Remote
$100K - $160K/yr
The RWE Statistician is involved in planning, conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database ...
... Statistician (LPS) for routine works in an established area (clinical/ observational studies, MA tactic, Biomarker & PK/PD Analyses or local project). The position can also act as a Senior ...
... Statistician (LPS) for routine works in an established area (clinical/ observational studies, MA tactic, Biomarker & PK/PD Analyses or local project). The position can also act as a Senior ...
Boston, MA · On-site
$75K - $80K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Quick apply
Boston, MA · On-site
$75K - $80K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$75K - $80K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$75K - $80K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · Hybrid
$75K - $80K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · Hybrid
$75K - $80K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site +1
$54K - $66K/yr
The statistical analyses varies across patient-level clinical trial data, observational study (real-world) data and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site +1
$54K - $66K/yr
The statistical analyses varies across patient-level clinical trial data, observational study (real-world) data and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$54K - $66K/yr
The statistical analyses varies across patient-level clinical trial data, observational study (real-world) data and published aggregate data. Our work involves a range of techniques such as basic ...
Quick apply
Boston, MA · On-site
$54K - $66K/yr
The statistical analyses varies across patient-level clinical trial data, observational study (real-world) data and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$54K - $66K/yr
The statistical analyses varies across patient-level clinical trial data, observational study (real-world) data and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$54K - $66K/yr
The statistical analyses varies across patient-level clinical trial data, observational study (real-world) data and published aggregate data. Our work involves a range of techniques such as basic ...
Be Seen First
Alameda, CA · Remote
$80 - $90/hr
Medical affairs, publication support, mainly use clinical studies database, Phase IV/open label studies or observational studies. Stat background is preferred. Job Summary (Primary function) The ...
Quick apply
Be Seen First
Alameda, CA · Remote
$80 - $90/hr
Medical affairs, publication support, mainly use clinical studies database, Phase IV/open label studies or observational studies. Stat background is preferred. Job Summary (Primary function) The ...
Boston, MA · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Quick apply
Boston, MA · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
New York, NY · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
New York, NY · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Boston, MA · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
New York, NY · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
Quick apply
New York, NY · On-site
$95K - $105K/yr
The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic ...
... observational studies. Working under the direction of the lead study statistician, this position implements pre-specified statistical analysis plans in R, contributes analytic content to the drafting ...
... observational studies. Working under the direction of the lead study statistician, this position implements pre-specified statistical analysis plans in R, contributes analytic content to the drafting ...
Princeton, NJ · On-site
$231K - $346K/yr
Demonstrated expertise in observational study design, statistical methods (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc), and RWD evaluation. * Hands-on ...
Princeton, NJ · On-site
$231K - $346K/yr
Demonstrated expertise in observational study design, statistical methods (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc), and RWD evaluation. * Hands-on ...
Demonstrated expertise in observational study design, statistical methods (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc), and RWD evaluation. * Hands-on ...
Demonstrated expertise in observational study design, statistical methods (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc), and RWD evaluation. * Hands-on ...
... statistical programming (R, SAS or equivalent acceptable) * 3 or more years ofexperience supporting clinical research studies, including observational studies, registries, and/or assay validation ...
... statistical programming (R, SAS or equivalent acceptable) * 3 or more years ofexperience supporting clinical research studies, including observational studies, registries, and/or assay validation ...
Princeton, NJ · On-site
$231K - $346K/yr
Demonstrated expertise in observational study design, statistical methods (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc), and RWD evaluation. * Hands-on ...
Princeton, NJ · On-site
$231K - $346K/yr
Demonstrated expertise in observational study design, statistical methods (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc), and RWD evaluation. * Hands-on ...
NC · Remote
Leads the statistical design, analysis, interpretation, and reporting of pharmacovigilance and safety-focused observational studies using complex longitudinal registry data Collaborates with ...
NC · Remote
Leads the statistical design, analysis, interpretation, and reporting of pharmacovigilance and safety-focused observational studies using complex longitudinal registry data Collaborates with ...
$50.5K - $56.5K
5% of jobs
$60.8K is the 25th percentile. Wages below this are outliers.
$56.5K - $62.5K
27% of jobs
$62.5K - $68.5K
1% of jobs
$68.5K - $74.5K
6% of jobs
$74.5K - $80.5K
1% of jobs
$80.5K - $86.5K
0% of jobs
$86.5K - $92.5K
0% of jobs
The median wage is $95.5K / yr.
$92.5K - $98.5K
18% of jobs
$102.5K is the 75th percentile. Wages above this are outliers.
$98.5K - $104.5K
24% of jobs
$104.5K - $110.5K
0% of jobs
$110.5K - $116.5K
17% of jobs
$50.5K
$86.9K
$116.5K
For Observational Study Statistician jobs, the most frequently searched job titles are:
King Of Prussia, PA • Remote
$100K - $160K/yr
Contractor
Medical, Dental, Life, Retirement, PTO
Posted 22 days ago
Purpose:
The RWE Statistician is involved in planning, conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database...), and/or large database .
The Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for real world evidence studies.
Key Responsibilities:
The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.
Study Design and Analysis
· Operate in collaboration with scientist in design studies and write protocols for the conduct of research projects.
· Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.
· Collaborate with data sciences in the planning and implementation of data quality assurance plans.
· Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
· Influence team members regarding appropriate research methods
· Perform peer-review of work products from other statistical colleagues.
Communication of Results and Inferences
· Collaborate with team members to write reports and communicate results.
· Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.
· Support responses to regulatory queries and/or regulatory interactions.
Therapeutic Area Knowledge
· Understand disease states, competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.
Regulatory Compliance
· Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.
Statistical leadership and Teamwork
· Introduce and apply innovative methodology and tools to solve critical problems
· Merge scientific thinking and business knowledge to identify issues, evaluate options and implement solutions.
Minimum Qualification Requirements:
§ Qualified Statistician (MSc, Ph.D). in Statistics OR Biostatistics with at least 3 years of experience in the pharmaceutical industry
§ Proven experience in conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database...), and/or large database
§ Prior experience in Rheumatology, Dermatology, or Gastroenterology would be an added value (but not mandatory)
Other Information/Additional Preferences:
· Proficient in statistical programming languages/software such as SAS and/or R
· Able to work in a virtual environment
· Teamwork and leadership skills
· Technical expertise and application with working knowledge of experimental design and statistical analysis
· Self-management skills with a focus on results for timely and accurate completion of competing deliverables
· Creativity and innovation
· Demonstrated problem solving ability and critical thinking
https://quantive.bio/
Sourced by ZipRecruiter
Biotechnology research and development
51 - 200 Employees
King of Prussia, PA, US
2000
