N-Power Medicine, Inc.

Accelerating Oncology Innovation

Senior Biostatistician

Clinical ResearchClinical ResearchFull TimeRemoteTeam 11-50H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

46 days ago

Salary

$186K - $259K / year

Postgraduate Degree5 yrs expEnglishPython

Job Description

• Build expert capabilities in prospective ECAs and hybrid controls combining retrospective and prospective real world-data with single arm and randomized controlled trials. • Provide expertise for developing statistical methodologies that mitigate selection, confounding, and measurement bias in external control and hybrid control studies. • Guide and mentor internal teams on novel methodologies, best statistical practices, and innovative clinical trial designs. • Collaborate with Clinical Science and Commercial teams for innovative clinical development projects. • Define data requirements and data collections processes to enable next generation ECAs. • Lead or support research study design and end-to-end delivery, including study scoping and development of study protocols. • Co-author communications of study results in peer-reviewed publications and presentations.

Job Requirements

  • 5+ years of industry/research experience or equivalent experience.
  • PhD in Statistics, or Biostatistics, or Related Field.
  • Expert knowledge of theoretical and applied statistics, including inferential methods for time-to-event analysis, survival analysis, and causal inference methods.
  • Expertise in design and analysis of externally controlled studies and hybrid controls including propensity score methods, endpoint measurement bias correction methods, and external patient borrowing bayesian and frequentest methods.
  • Fundamental understanding of clinical- and efficacy endpoints used in oncology development.
  • Experience collaborating with clinical-, biomarker-, and imaging scientists, to apply statistical methods to oncology drug development.
  • Extensive experience with programming in R and/or Python.

Benefits

  • equity at hire
  • discretionary annual bonus based on Company performance
  • company benefits
  • flexible work environment
  • competitive industry benefits
  • 401K plan
  • company perks

Related Categories

Related Job Pages

More Clinical Research Jobs

Clinical Research47 days ago
Full TimeRemoteTeam 11-50Since 2017H1B No Sponsor

Principal Clinical Scientist contributing to EFX clinical development initiatives

United States
$148.3K - $259.5K / year
Clinical Research47 days ago
Part TimeRemoteTeam 10,001+H1B Sponsor

Coordinates clinical research projects for patient-focused services in healthcare

Google Cloud Platform
Colorado
$67.7K - $115.1K / year

Director, Clinical Project Management

IMMUNEERING CORPORATION

Immuneering is an equal opportunity employer. We are committed to creating a diverse and inclusive workplace where all employees are treated with fairness and respect. We do not discriminate on the basis of race, ethnicity, color, religion, gender, sexual orientation, age, disability, or any other legally protected status. Our hiring decisions and employment practices are based solely on qualifications, merit, and business needs. We encourage individuals from all backgrounds to apply and join us in our mission.

Clinical Research48 days ago
Full TimeRemote

The Director of Project Management will oversee and drive the execution of global clinical trials in oncology. This leadership role is responsible for ensuring the successful planning, implementation, and completion of complex clinical programs, collaborating with cross-functiona...

Project ManagementClinical Trials ManagementOncology DevelopmentRegulatory ComplianceICH-GCPFDA RegulationsEMA RegulationsClinical Data ManagementVendor ManagementCross-Functional LeadershipRisk Management
United States

(Associate) Director, Clinical Scientist

IMMUNEERING CORPORATION

Immuneering is an equal opportunity employer. We are committed to creating a diverse and inclusive workplace where all employees are treated with fairness and respect. We do not discriminate on the basis of race, ethnicity, color, religion, gender, sexual orientation, age, disability, or any other legally protected status. Our hiring decisions and employment practices are based solely on qualifications, merit, and business needs. We encourage individuals from all backgrounds to apply and join us in our mission.

Clinical Research48 days ago
Full TimeRemote

Provide scientific and strategic leadership in the planning and execution of clinical trials, including protocol development, study design, and data analysis. Author and review clinical protocols, ICFs, CSRs and regulatory documents. Collaborate closely with cross-functional team...

Protocol DevelopmentClinical Trial DesignClinical Data AnalysisClinical Document WritingRegulatory SubmissionsOncology Clinical TrialsCross-Functional CollaborationCRO ManagementICH-GCPClinical Development StrategyPharmacologyBiostatistics
United States