Senior statistical analyst job description

Chubb is the world's largest publicly traded property and casualty insurer.With operations in 54 countries, Chubb provides commercial and personal property and casualty insurance, personal accident and supplemental health insurance, reinsurance and life insurance to a diverse group of clients.

Implement external statistical plan changes by identifying the revision, initiating contact with the proper internal areas, maintaining open communication and analyzing test data.

Prepare and submit non-workers compensation data calls to the appropriate regulatory authorities.Analyze data requirements for changes and implement any resulting revision.Write and execute data extracts from various source systems to support the preparation of the data calls.

Identify data quality deficiencies, and the underlying causes, and initiates corrective action which can result in greater cost effectiveness, improved management information and/or conformance to established data quality standards.Respond to any statistical agent data inquiries in accordance with department standards.

Monitor changes within the company regarding new business, new systems, or other changes that might impact the reports.
Reconcile Data Calls to Financials. Monitors fluctuations in summarized statistical data to identify areas requiring further investigation and coordinates the resolution of significant deviations in the data. Monitor, analyze and take corrective action of transaction level data error records and/or suspense items. Self-motivated with the ability to work independently Ability to identify process improvements and successfully present to management.
Assist in large corporate initiatives ensuring that statistical reporting requirements are addressed. Includes representing the department's interest at large, multi-departmental meetings on an on-going basis and analyzing, responding and documenting test data to various internal/external areas.
Work with various regulatory authorities including the departments of insurance and/or statistical agents.Work with various internal departments including Office of General Counsel, Data Management and Actuarial. Working with minimal supervisory guidance to understand required process and state specific learning.



Qualifications:



Qualifications:



Bachelor's degree and/or 5-10 years' experience in Regulatory Reporting required. Demonstrated knowledge of Property & Casualty Insurance Extensive knowledge in Non-Workers Comp Data Call requirements and preparation. Advanced analytical ability in a data intensive environment. Advanced analytical and problem solving skills with the persistence to resolve them completely in a data intense environment that is results oriented. Strong work ethic with the ability to work independently with minimal supervision. Excellent oral and written communication skills. Excellent organizational skills. Ability to handle multiple priorities within strict time constraints and possess the ability to identify and prioritize work load. Excellent interpersonal skills. Ability to communicate and negotiate with external agencies (e.g. ISO, CAR, Statistical Agents, Insurance Departments, etc.). Problem ownership and personal responsibility of assigned work. Excellent time management skills required. Experience in process review and documentation. Comfortable interacting with multiple levels of management and peers. Advanced knowledge of Excel, Word, Microsoft Access, Cognos, SQL, QlikView and various extract tools required.



Chubb strives to offer a diverse and inclusive and rewarding work environment.Teamwork and mutual respect are central to how Chubb operates and we believe the best solutions draw upon diverse perspectives, experiences and skills.We operate in such a way where everyone, regardless of their singular background has the opportunity to contribute to our collective success.

Who We Are:
At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs, but few options.

What We Do:
Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. *in collaboration with AbbVie

About the Role:
Designs, develops, tests, maintains, validates, and documents SAS programs to evaluate clinical data and meet the project requirements for SAS statistical programming efforts for clinical and non-clinical projects and studies. Provides technical expertise to the development of programming standards and procedures.
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Your Contributions (include, but are not limited to):
Serves as the primary project team representative, delegating work as appropriate
Generates SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data
Reviews output across programs to ensure consistency
Reviews maintains and approves study documents per standard procedures
Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures
Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting
Participates in the development and/or maintenance of departmental procedures and standards
Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures
Implements data management plans designed to meet project and protocol deadlines
Acts as a liaison between clinical management, subcommittees and project teams as needed
May train and mentor new programmers
Performs other duties as assigned

Requirements:
BS/BA degree in computer science, mathematics, statistics, or related discipline and 6+ years experience in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph). In addition, must have at least three years of experience serving in a supervisory or lead capacity. Experience managing projects ORMaster's degree in computer science, mathematics, statistics, or related discipline and 4+ years of similar experience noted above ORPhD in computer science, mathematics, statistics, or related disciplineand 2+ years of similar experience noted above Demonstrates strong knowledge with industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines Strong understanding of relational databases and experience working with complex data systems. Strong knowledge of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems. Strong knowledge of SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains. Strong programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar Understands key business drivers and uses this understanding to accomplish work Has strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas Proficient with tools and processes that support work conducted by functional area Ability to work as part of a team; may train lower levels Excellent computer skills Strong communications, problem-solving, analytical thinking skills Detail oriented yet can see broader picture for department Ability to meet multiple deadlines, with a high degree of accuracy and efficiency Strong project management skills Strong interpersonal skills to effectively work in a team environment Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines Proficiency with Word, Excel, and PowerPoint is required as is the ability to communicate effectively both verbally and in writing

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Neurocrine Biosciences is an EEO/AA/Disability/Vets employer.

As a condition of employment with Neurocrine Biosciences, Inc. in the United States, you must be fully vaccinated for COVID-19 and provide valid proof of vaccination to the company.