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.
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.
Serve as Study Biostatistician for assigned clinical trials to provide statistical support from design, analysis to reporting
Collaborate with cross-functional experts on clinical trial designs and make contributions to determination of objectives, endpoints and sample size
Conduct data analyses as needed by using own SAS programs in collaboration with internal Statistical Programming team
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, they are continuously expanding their presence and global footprint and searching for high-impact individuals to strengthen their patient-centric team.
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.
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.
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.
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.
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.