Lead Biostatistician
Thermo Fisher ScientificSalary not specified
- Full Time
- Junior (1 to 2 years)
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Biotechnology, HealthcareIndustries
Requirements
Candidates should have over 5 years of experience in statistics or biostatistics within the clinical or medical research field. Extensive experience with statistical programming tools such as SAS or R, along with knowledge of regulatory guidelines including CDISC standards, is required. Strong leadership abilities with experience in managing reports, leading teams or projects, and providing mentorship are essential. Exceptional written and verbal communication skills to convey complex statistical findings to diverse audiences are necessary. The candidate must be able to work independently while managing multiple projects and priorities and should have a passion for the healthcare industry and commitment to driving innovative treatments.
Responsibilities
The Senior Biostatistician will lead the statistical strategy design and take ownership of statistical strategy and analysis for clinical trials across multiple therapeutic areas and phases. They will create and implement statistical Standard Operating Procedures and collaborate closely with sponsors and the Clinical Operations teams to ensure tailored solutions. The role includes leading statistical programming efforts for complex clinical trials, ensuring high-quality analysis and reporting. Additionally, the Senior Biostatistician will serve as an internal Subject Matter Expert for statistical methodologies, trial design, and data management, providing guidance to cross-functional teams and external stakeholders. They will also be responsible for line managing and mentoring junior team members and helping to develop internal processes and best practices to ensure high-quality results.
Skills
SAS
R
Statistical Programming
Clinical Trials
Biostatistics
CDISC Standards
Statistical Strategy
Statistical Analysis
Statistical Reporting
Trial Design
Data Analysis
Lindus Health
Accelerates clinical trials for life sciences
About Lindus Health
Lindus Health focuses on speeding up clinical trials to help patients access new treatments more quickly. The company operates differently from traditional contract research organizations (CROs) by using a fixed-price model for studies and milestone-based payments, which aligns their incentives with those of their clients. Lindus Health combines a skilled clinical operations team with a specialized software platform and access to a vast database of 30 million Electronic Health Records. They handle all aspects of clinical studies, including designing the study, recruiting patients, capturing clinical data, monitoring progress, and managing projects. With their approach, Lindus Health has successfully assisted over 90 sponsors in conducting clinical trials across the US, UK, and Europe, completing them up to three times faster than conventional CROs and often delivering results ahead of schedule.
Key Metrics
London, United KingdomHeadquarters
2021Year Founded
$23MTotal Funding
SERIES_ACompany Stage
Biotechnology, HealthcareIndustries
51-200Employees