Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Provide statistical programming leadership to support analysis and reporting for assigned clinical programs.
Lead a group of Statistical Programmers to deliver while also being hands-on.
Work closely with biostatisticians for data analysis, vendor supervision and provide programming leadership to support Definium’s integrated data analyses.
Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Founded in 2019, we are continuously expanding our presence and global footprint, looking for high-impact individuals.
Provide statistical leadership for clinical and/or consumer health studies
Develop and review Statistical Analysis Plans (SAPs)
Contribute to study design, including sample size calculation and protocol development
ClinChoice specializes in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries and aim to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
Provide strategic and technical leadership to support and lead statistical activities for clinical trials across multiple studies.
Lead the development and review of statistical deliverables, including protocols, SAPs, TFLs, ISS/ISE, and regulatory submission materials.
Serve as a key statistical representative in cross-functional team discussions and governance meetings
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. ClinChoice considers their employees the most valuable company asset and focuses on close management and training to develop highly-qualified personnel.
Consult and collaborate on clinical research studies.
Participate in grant preparation and protocol development.
Analyze data using statistical software (SAS, R).
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. They welcome candidates who can contribute to the excellence of their academic community.
Design research studies and clinical trials, determining the necessary sample size and planning how to collect accurate and reliable data.
Extract, store, and prepare large datasets for analysis, including cleaning and reorganizing existing data.
Use sophisticated statistical models and techniques to analyze data, often dealing with complex structures and missing values to find meaningful patterns and relationships.
Lucile Packard Children’s Hospital Stanford combines advanced technologies and breakthrough discoveries with family-centered care. They provide caregivers with continuing education and state-of-the-art facilities.
Attend multi-disciplinary team meetings, representing the statistical programming function.
Review and approve SAPs and TFL shells before the start of programming outputs
Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
Celcuity is a clinical-stage biotechnology company focused on developing targeted therapies for cancer, particularly solid tumors. The company's lead candidate, gedatolisib, is in Phase 3 clinical development and they also have ongoing Phase 1b/2 trials.
Help with statistical programming tasks for clinical trials.
Create CDISC data sets and tables/figures/listings.
Ensure high-quality statistical analyses for decision-making and submissions.
Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients. They are advancing their pipeline of off-the-shelf, or allogeneic, cell therapies from their CAR-T cell therapy platform.
Assist senior biostatisticians in clinical study support.
Support the statistical aspects of case report form design.
Write data quality control specifications and utilize computer languages and software.
Jobgether is a platform that connects job seekers with employers. They utilize AI to match candidates with the right opportunities and streamline the hiring process for companies looking for talent.
Design, prepare data, and conduct analysis and delivery of RWE analyses for biopharma clients.
Translate complex clinical development and translational research questions into actionable research plans and insights utilizing Natera data for trial design, outcomes research and other bespoke projects.
Generate insights from complex real-world endpoints demonstrating deep comprehension of Natera clinical and molecular data structures and complexity.
Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Natera's team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for the work and each other.