Associate Director, Statistical Programming

Location
San Francisco, CA, United States
Posted
Sep 28, 2018
Ref
3376-525-2018
Hotbed
Biotech Bay
Required Education
Bachelors Degree
Position Type
Full time
Position Overview

Provide strong technical statistical programming leadership to Statistical Programming function within BDM and be a technical resource for statistical programmer analysts.

Serve as mentor to statistical programmers. Lead technology or process initiative. Lead the design or development of global utilities and macros. Provide expertise and hands on support to clinical projects across multiple therapeutics areas. Contribute in Building Statistical Programming Infrastructure. This job contributes to and supports the company's research and development efforts to create high value therapeutics to address unmet medical needs.

Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgments within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Ensures budgets, schedules and performance requirements are met. Work with IT ensuing that local IT infrastructure meets Biometrics needs and global standards. Adhere to principles of GCP * Develop, apply and promote consistent programming standards through standard processes and SOPs. Identify areas of deficiency requiring SOPs or guidelines and develop and execute a plan to rectify. Administratively and functionally manage statistical programmers with respect to statistical programming strategy, deliverables, processes, and professional development. Lead standardization efforts (CDSIC, ADaM, and Define.xml) per EMA/FDA submission requirments. Provide timeline and resource forecasts for statistical programming deliverables. Mentor statistical programmers on team performance and relevant therapeutic areas. Responsible for processing of clinical data required for analysis of clinical trials for Phase 1-4. Initiate programming environment. Develop SAS coding and table templates for preparing, processing and analyzing clinical data. Create/acquire tools to improve programming efficiency or quality. Validate work of other programmer/analysts at CRO or in-house. Perform vendor qualifications. Manage CRO regarding programming issues and activities to ensure timely delivery of tables and data listings. Provide guidelines, review, and QC CRO deliverables to ensure the quality of deliverables. Participate in the lead task forces and new initiatives, while maintaining current knowledge of programming practices and development within the industry. Work with other functional groups to identify areas where statistical programming support can enhance efficiency and quality. Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues. Ensure SOPs have been developed properly. Ensure statistical programming tasks has been conducted in a compliant and timely manner with high qulaity across all projects. Ensure the computer system and network are set up approporitely. Administratively and functionally manage statistical programmers with respect to statistical programming strategy, deliverables, processes, and professional development. Lead standardization efforts (CDSIC, ADaM, and Define.xml) per EMA/FDA submission requirment. Provide timeline and resource forecasts for statistical programming deliverables. Mentor statistical programmers on team performance and relevant therapeutic areas.

A minimum of a Bachelor's degree in Computer Science, Mathematics, Statistics, and related areas is required. A Masters or PhD is preferred. Equivalent experience may be accepted. A minimum 12 years relevant career experience in the pharmaceutical or biotechnology industry. A minimum 5 years experience managing statistical programming group and activities Excellent knowledge of SAS programming and associated features and their applications in pharmaceuticals industry environment in particular clinical trial data setting. Experience with Clinical Study Reports and NDA submissions. Expert at senior statistical programmer level in a pharmaceutical or CRO working in a FDA regulated environment. Excellent knowledge of ICH, FDA, and GCP regulations and guidelines. Strong well-rounded technical skill, SAS, CDISC, Submission CRTs. Customer & Industry Knowledge. Advanced knowledge of FDA, EMA, and ICH guidances; CDISC and ADaM and electronic submissions. Advanced knowledge of integrated summary of data. Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results. Thorough understanding of relational database components and theory. Excellent oral and written communication skills.

We are an Equal Opportunity Employer and do not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class. Nektar Therapeutics will consider for employment qualified applicants with criminal histories in the manner proscribed by the San Francisco Fair Chance Ordinance.