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Senior Consultant, Statistics and Psychometrics
Lifelancer. Lead the quantitative analysis workstream for projects of moderate complexity .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in advanced statistical methods for clinical outcome assessment and patient-reported outcomes, with a strong focus on regulatory evidence generation and effective communication of complex analyses. Proven ability to lead quantitative analysis projects while mentoring junior team members and managing deliverable quality.
Highest-signal resume keywords
Advanced Statistical MethodsBiostatisticsSASRClinical Trials
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Multivariate AnalysisRegression AnalysisLogistic AnalysisSurvival AnalysisMixed Models Repeated Measures
Soft Skills
Excellent Communication SkillsAttention to DetailCollaborative Work Style
Certifications & Qualifications
Master’s DegreePhD
Industry Keywords
PharmaceuticalBiotechCROHealthcareConsulting
About the role
Key responsibilities & impact- Lead the quantitative analysis workstream for projects of moderate complexity
- Develop and review analysis plans, output shells, output specifications, programming requirements, statistical outputs, and technical reports
- Apply advanced statistical methods to clinical outcome assessment and patient-reported outcomes data
- Interpret results for internal teams and clients
- Communicate methodological choices to support decision-making
- Contribute to regulatory- and payer-relevant evidence generation, endpoint strategy, and scientific communication
- Build relationships with clients and cross-functional internal teams
- Contribute to proposals, bid defenses, and business development activities
- Assist in managing workstream objectives, timelines, and deliverable quality
- Mentor junior team members and contribute to training, standards, and process improvement
Requirements
What you’ll need- Master’s degree or PhD in biostatistics, statistics, psychometrics, outcomes research, epidemiology, or a related quantitative field
- 5+ years of relevant experience in the pharmaceutical, biotech, CRO, healthcare, or consulting environment
- Advanced knowledge of complex statistical methods applicable to Phase I-IV clinical trials, including multivariate analysis, regression analysis, logistic analysis, survival analysis, and mixed models repeated measures
- Familiarity with SAS and/or R
- Excellent written and verbal communication skills
- Strong attention to detail
- Ability to work effectively in a collaborative, matrixed environment
- This role is not eligible for UK visa sponsorship
Benefits
Comp & perks- Opportunity to work on specialized, patient-centered research across a wide range of therapeutic areas
- Collaborative global team with deep expertise in COA analysis, psychometrics, and advanced statistical methodology
- Training, standards, and process improvement contributions
- Mentorship and team capability-building opportunities
- Diversity, inclusion, and belonging culture
- Opportunity to contribute to high-impact clinical development, regulatory strategy, and evidence communication