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Principal Statistician - Real World Analytics

Role overview

Qualifications

  • PhD or MS in Biostatistics or Statistics
  • Experience in pharmaceutical industry for statistical input on study design and analysis
  • Min 4 yrs experience with Phase-4 studies or Real World Evidence (RWE)
  • Min 4 yrs experience in statistical software, SAS and R

Responsibilities

  • Provide statistical support in protocol development for observational studies and/or clinical trials
  • Author and review statistical analysis plans and analysis dataset specifications
  • Work with cross-functional teams in Phase-4 non-interventional study to develop CRF
  • Conduct programming and analysis for Medical Affairs, RWE studies

Key facts

  • Remote from: Anywhere
  • Full time
  • Senior (5-10 years)
  • Statistician
  • English

Hard skills

Other skills

  • Collaboration
  • Communication

About the company

Aequor Technologies logo

Aequor Technologies

IT Services & IT Consulting

Since 1998, Aequor has provided exceptional workforce staffing services in multiple industries. Specializing in healthcare, we place nurses, therapists, allied professionals, physicians and medical technicians, as well as staff in the life sciences, technologies and schools. We believe in making a positive impact in the lives of those we serve by inspiring people and empowering growth both personally and professionally, which makes us better as individuals and as a company. We teach our team members to nurture positive and supportive relationships with our clients and candidates by nurturing positive and supportive relationships with each other—from the desk level to the C-suite.Year after year, Aequor is awarded for being one of the best places to work—for the candidates we place in assignments all over the country, and for our internal team, the Aequor Family. The vibrant culture of community and support that welcomes each new team member is the same culture that makes them want to stay. We understand that we’re better in collaboration rather than competition, so we build each other up, respect each other, and show up for one another.As a thriving healthcare staffing firm committed to investing in the resources and tools that ensure a remarkable experience for our clients, candidates and team members, Aequor’s personal approach connects the workforce needs of the industry with the right talent for the job.

Company details

Company typeLarge
IndustryIT Services & IT Consulting
Company size201 - 500

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Job description

  1. Screening Requirements, 1. Basic Background 2. 11 Panel Drug + Fentanyl

Core Essential Skill sets:
1. Education: PhD or MS in Biostatistics or Statistics
2. Experience in pharmaceutical industry to provide statistical input into the study design, statistical analysis, and reporting of interventional and observational studies.
3. Min 4 yrs experience with Phase-4 study, Medical Affairs study, Real World Evience (RWE) or HEOR study.
4. Min 4 yrs experience in statistical software, SAS and R.
5. Min 4 yrs experience with SDTM and ADaM data standards.
6. Min 4 yrs experience with Real World Data (RWD) and RWE methodologies, such as propensity score analysis, causal inference.
7. Min 4 yrs experience with advanced statistical models such as mixed effect model approaches for repeated measures, Machine Learning (ML) methods.

Position Summary:
• Provide statistical support in protocol development for observational studies and/or clinical trials.
• Author and review of statistical analysis plans, analysis dataset specifications, and TFL shells.
• Work with programming and other cross-functional teams in Phase-4 non-interventional study to develop CRF, validate and review the datasets and results.
• Conduct programming and analysis for Medical Affairs, RWE studies.
• Support develop abstract, poster and manuscript as deliverables.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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