div class="flex max-w-full flex-col grow">li>Maintain policies and protocols for the MA in Statistics program in alignment with the University, GSAS, and departmental policies, calculate the annual operation budget of the MA in Statistics program, and plan year-round program activities to ensure that the program meets essential milestones each year; carry out annual reviews of the program each summer and propose programmatic and operational improvements for the next academic year. Reporting to the Department Chair and Vice Chair for MA Programs, the Director of MA Programs will be expected to direct the operational and administrative aspects of the Statistics Master's program, and to coordinate the statistics department involvement with their partner MA programs, including MAFN, MS-DS, MS-AI, Actuarial Science, QMSS, and subsequent programs the department may be involved in.
They contribute to the formulation and implementation of monetary policy, the supervision of financial institutions, the smooth operations of the payments system, the analysis of the impact of policies on consumers and communities and the way in which the financial system supports economic growth using insights from macroeconomics, microeconomics asset pricing and corporate finance. Candidates who are not U.S. citizens or U.S. permanent residents may be eligible for the information access required for this position and sponsorship for a work visa, and subsequently for permanent residence, if they sign a declaration of intent to become a U.S. citizen and meet other eligibility requirements.
Somerset, New Jersey30+ days ago
Led by former FDA experts and industry experts, R&G US can provide end-to-end services in strategic planning, clinical trial design, statistical analysis, SAS programming, data management, medical writing, medical monitoring, pharmacovigilance, and Data Monitoring Committee services. R&G US's goal is to provide the best service to the clients and work as one team to lower costs, shorten development time, and increase the success probability of products.
p>For ideas about how you might be able to protect yourself from job scams, visit our scam-awareness page at https://careers.progressive.com/pages/how-we-hire-faq-job-scams/. In this dynamic role, you'll navigate complex claims data to deliver actionable insights, share best practices with other analytical groups, as well as collaborate with business groups such as product and corporate reserves.
li> Provides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing. Responsibilities: Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
Foreign Education: If your transcripts show education completed in foreign colleges or universities, you must also provide documentation that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in a conventional/accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. Specialized Experience for GS-13 is work that primarily consists of: (1) overseeing studies involving large datasets comprised of messy data and statistical or machine learning analytical techniques and processes; (2) transforming data into a form suitable for analysis using R, Python, SAS, or SQL; (3) summarizing projects in writing for technical and non-technical audiences.
You will also play a key role in contributing to business development by developing and maintaining excellent client relationships and identifying opportunities to provide additional services to clients within projects. To learn more about the personal and professional development opportunities at Costello Medical, explore first-hand career profiles from our colleagues about their experiences with the company: https://www.costellomedical.co.uk/careers/working-at-costello-medical/.
Statistician Katalyst Healthcares & Life Sciences
StatisticianJersey, NJ23 days ago
Provides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing. Responsibilities: Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
div> Job Summary: The Senior Manager Statistics will be responsible for statistical activities across all stages of clinical trials, from protocol development through final study reporting.
Review CRFs, database design, and edit check specifications to ensure data integrity and consistency.
Degree: that included 15 semester hours in statistics (or in mathematics and statistics, provided at least 6 semester hours were in statistics), and 9 additional semester hours in one or more of the following: physical or biological sciences, medicine, education, or engineering; or in the social sciences including demography, history, economics, social welfare, geography, international relations, social or cultural anthropology, health sociology, political science, public administration, psychology, etc. Credit toward meeting statistical course requirements should be given for courses in which 50 percent of the course content appears to be statistical methods, e.g., courses that included studies in research methods in psychology or economics such as tests and measurements or business cycles, or courses in methods of processing mass statistical data such as tabulating methods or electronic data processing.
In six years since inception, we've created eight enduring companies and over $1B in enterprise value, including the leading deidentified healthcare data exchange platform (Datavant) and a top-tier computational drug discovery company (VantAI) which has partnered with Johnson & Johnson, Bristol-Myers Squibb, and Boehringer Ingelheim. Five new medicines have been approved off the Roivant platform, we''ve built multiple biotechs that have become public companies, and we''ve created substantial value across the platform spanning computational drug discovery, healthcare data exchange, and novel therapeutic platforms.
Princeton, NJ30+ days ago
For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. The Role : The Senior Director acts as a high-level statistical expert supporting the clinical development of compounds as therapeutic area lead, compound lead and/or indication lead for both early and late-stage programs and may also act as trial responsible statistician with responsibilities as described below.
This role will be working directly with Sales, Revops and Marketing stakeholders to understand their analytical needs, build the data infrastructure to support them, and surface insights that move the business forward. Familiarity with CRM and GTM tooling: Salesforce (required)- you understand the data model and can navigate SFDC objects and fields ,HubSpot, GA4 Mixpanel, and/or Stripe experience is a strong plus.
Required Skills: Clinical Trials Operations, Cross-Functional Leadership, Executive Leadership, Pharmaceutical Industry, Program Management, Project Management, Regulatory Compliance, Reporting Processes, Software Development Life Cycle (SDLC), Statistical Analysis, Statistical Programming, Statistics, Vendor Management. Primary Responsibilities: Leads the delivery of analysis and reporting tools, processes, platforms, and training for Biostatistics and Research Decision Sciences (BARDS) staff supporting all clinical trial phases and therapeutic areas, with a focus on regulatory compliance, quality, and efficiency.
As required by the California, Colorado, Hawaii, Illinois, Maryland, Minnesota, New Jersey, New York State, New York City, Vermont, Washington State, and Washington DC laws, the pay range for this position is as follows: The minimum full-time salary range is between $60,000 - $70,000. The Specialist, Measurement will use their knowledge of data management, statistical programming, quality assurance procedures, and statistical reporting to support the development of licensure and certification exams and ensure quality of data files and technical reports.