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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading early phase clinical trials and statistical analysis, with proficiency in SAS and R for inferential statistics. Capable of mentoring junior statisticians and improving internal processes while effectively managing client interactions and timelines.
Highest-signal resume keywords
Biostatistical ExperienceSAS ProgrammingStatistical Analysis Plans (SAPs)Leadership in Clinical TrialsClient Facing Responsibilities
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
BiostatisticsStatistical AnalysisInferential StatisticsStatistical MethodsStatistical ProgrammingClinical Trials ManagementProtocol DevelopmentData AnalysisStatistical ReportingTimeline Management
Soft Skills
Effective CommunicationLeadership AbilityTime ManagementMentoring SkillsPrioritization
Certifications & Qualifications
Master's Degree in BiostatisticsPh.D in Biostatistics
Industry Keywords
Clinical Research Organization (CRO)PharmaceuticalBiotechRegulatory AgenciesClient Interactions
About the role
Key responsibilities & impact- Lead and oversee early phase clinical trials
- Provide input to statistical components including protocols, mocks/shells, SAP text, programmed deliverables, and CSRs
- Serve as lead biostatistician for programs of studies, or on simple to complex individual studies
- Oversee statistical activities that support ICON’s interactions with clients and regulatory agencies
- Review and approve statistical methods sections of study protocols
- Author statistical analysis plans (SAPs), and statistical input to reports
- Program using SAS and/or R for inferential statistics
- Conduct statistical analyses for clients
- Mentor or provide support to junior statisticians
- Lead or partake in initiatives to improve internal processes or create new guidance
Requirements
What you’ll need- Master's degree OR Ph.D in Biostatistics, Statistics, or a related field
- 5+ years of biostatistical experience in either a CRO, pharmaceutical, or biotech company
- Experience leading studies, including client facing responsibilities and timeline management
- Experience working in a clinical research organization (preferred)
- Advanced ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical studies
- Effective written and verbal communication skills with demonstrated leadership ability
- Ability to prioritize with strong time management skills
- Legal right to work in the country where the role is based
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways