Statistical Associate Cover Letter

In response to your job posting for statistical associate, I am including this letter and my resume for your review.

In the previous role, I was responsible for statistical sciences training to UCB employees from different disciplines on advanced statistical concepts.

Please consider my qualifications and experience:

• PhD in statistics, mathematics or closely related fields
• Experience leading large and/or complex statistical programming projects that include coordinating/directing the activities of a programming team with US and/or worldwide drug or vaccine regulatory application submission experience including the development of CRT SDTM study data standard deliverables
• Superior knowledge of study data standards CDISC (SDTM), Define.XML, SDRG, aCRF
• Expertise in SAS and clinical trial programming
• Excels in technical writing, able to convert complex ideas and information into simple readable form
• Familiarity with statistical and clinical data management concepts
• US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development of CRT SDTM study data standard deliverables
• Strong knowledge and experience with study data standards CDISC CDISC (SDTM), Define.XML, SDRG, aCRF

In response to your job posting for statistical associate, I am including this letter and my resume for your review.

In my previous role, I was responsible for technical guidance to statistical programmers and vendors around GBDS conventions, standards, practices, and specifications to ensure integrated computing solutions.

Please consider my experience and qualifications for this position:

• Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH
• Experience in CDISC SDTM and ADaM standards
• Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters)
• Good understanding of basic statistical methodology
• Experience with small and simple projects preferred as well
• Knowledge of clinical trials structure
• Extensive knowledge of drug development process and regulatory requirements
• Proven experience in managing a group of statistical programmers across several drug programs

I submit this application to express my sincere interest in the statistical associate position.

In the previous role, I was responsible for predictive analytics and modeling services using statistical, data mining, and actuarial/financial methods and processes to produce profitable growth and retention.

Please consider my experience and qualifications for this position:

• Regular sitting for extended periods
• Proven knowledge and expertise in statistical analyses, and strong computer skills with experience in statistical software such as SAS or other analytical tools
• Good working knowledge of SAS programming language
• Knowledge of statistical concepts in support of analyses and reporting
• Knowledge of new advanced statistical methods using R and SAS
• Experience working as part of a software development team and fundamental SDLC processes
• Will have people management responsibilities
• Ensures that software development lifecycle practices are followed and document as specified by our SOPs and best practices

In response to your job posting for statistical associate, I am including this letter and my resume for your review.

In my previous role, I was responsible for assistance in explaining technical actuarial results to various actuarial / non-actuarial audiences, particularly opportunity to interface with corporate, finance, accounting policy, and risk functions within Voya.

Please consider my experience and qualifications for this position:

• Ensures appropriate documentation is generated to support audit readiness in defense of our standard software development
• Excellent communication skill to ensure appropriate collaboration with statisticians, data managers, statistical programmers, clinical pharmacology leads, research data scientists and programming leads to ensure clear specifications for their programmed deliverables are in place
• Clinical trials data flow expertise from data collection through reporting
• Experience working with a global programming team for necessary deliverables
• May contribute to department level initiatives
• Working knowledge of clinical data and relevant data standards
• Knowledge of at least 1 Therapeutic Area
• Experience with common NGS bioinformatic tools (Bowtie, SAMtools, bwa, ) and/or major genome database resources

I am excited to be applying for the position of statistical associate. Please accept this letter and the attached resume as my interest in this position.

In my previous role, I was responsible for statistical and strategic input in the writing of Statistical Analysis Plans (SAPs) and Integrated SAPs, and for pooling strategies for regulatory submissions.

My experience is an excellent fit for the list of requirements in this job:

• Proven experience in developing direct reports
• Excellent leadership skills, including collaboration and influence with key stakeholders and senior leadership
• Detailed understanding of automatic data processing, including R
• Knowledge of general principles related to statistics and data management analysis
• Knowledge of computing applications such as SAS/STAT and Python
• Education and/or work experience in statistical analysis
• Training/experience in data visualization tools such as Tableau
• Training/experience in geographic information systems