Everest Clinical Research Services Inc.
Associate Director, Statistical Programming
Everest Clinical Research Services Inc., Trenton, New Jersey, United States,
Associate Director, Statistical Programming
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as
Associate Director, Statistical Programming
for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.Job Accountabilities:Work with a Director, Senior Director, and/or Executive Director of Biostatistics/Biometrics to manage clinical trial programs/projects from one or multiple clients.Provide day-to-day technical and operational leadership to project teams supporting these programs/projects.Represent the company and the Statistical Programming department in business development and client relationship management initiatives.Provide leadership and oversight to the assigned client programs/projects; ensure quality, timely, and within budget deliveries.Follow-up on the industry trends in data and programming standards and good programming working practices.Develop and maintain clinical data and statistical reporting standards in line with pharmaceutical industry standards and conventions.Coach, mentor, develop, and provide technical review, advice, and expertise to direct subordinate Statistical Programmers, as well as indirect subordinate Biostatisticians and Statistical Programmers assigned to the program/projects.Perform semi-annual and annual performance review and create developmental plans for direct subordinates and, where appropriate, indirect subordinates.When required, serve as a principal level Statistical Programmer, working effectively with interdisciplinary teams to contribute strategically to drug development and commercialization.Perform quality control (QC) review of statistical programming deliverables, including documentation, before they are released for production or delivered to clients.When required, review and provide input to clinical data management deliverables.Contribute to organization development and growth by participating in the interview and evaluation process for professional applicants.Qualifications:Must have at least a bachelor degree and preferred to have M.Sc., M.A. or higher in Statistics, Computer Science, or relevant fields with at least 14 years of clinical research experience.Requires demonstrated experience in leading statistical programming teams.Requires demonstrated experience implementing CDISC standards.Requires demonstrated experience supporting electronic regulatory submissions.Experience with multiple regulatory agencies preferred.Exceptional people management skills.Exceptional written communication and presentation skills.Travel level specification:
This position may require up to 10% business travel.We thank all interested applicants, however, only those selected for an interview will be contacted.Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities.
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Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as
Associate Director, Statistical Programming
for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.Job Accountabilities:Work with a Director, Senior Director, and/or Executive Director of Biostatistics/Biometrics to manage clinical trial programs/projects from one or multiple clients.Provide day-to-day technical and operational leadership to project teams supporting these programs/projects.Represent the company and the Statistical Programming department in business development and client relationship management initiatives.Provide leadership and oversight to the assigned client programs/projects; ensure quality, timely, and within budget deliveries.Follow-up on the industry trends in data and programming standards and good programming working practices.Develop and maintain clinical data and statistical reporting standards in line with pharmaceutical industry standards and conventions.Coach, mentor, develop, and provide technical review, advice, and expertise to direct subordinate Statistical Programmers, as well as indirect subordinate Biostatisticians and Statistical Programmers assigned to the program/projects.Perform semi-annual and annual performance review and create developmental plans for direct subordinates and, where appropriate, indirect subordinates.When required, serve as a principal level Statistical Programmer, working effectively with interdisciplinary teams to contribute strategically to drug development and commercialization.Perform quality control (QC) review of statistical programming deliverables, including documentation, before they are released for production or delivered to clients.When required, review and provide input to clinical data management deliverables.Contribute to organization development and growth by participating in the interview and evaluation process for professional applicants.Qualifications:Must have at least a bachelor degree and preferred to have M.Sc., M.A. or higher in Statistics, Computer Science, or relevant fields with at least 14 years of clinical research experience.Requires demonstrated experience in leading statistical programming teams.Requires demonstrated experience implementing CDISC standards.Requires demonstrated experience supporting electronic regulatory submissions.Experience with multiple regulatory agencies preferred.Exceptional people management skills.Exceptional written communication and presentation skills.Travel level specification:
This position may require up to 10% business travel.We thank all interested applicants, however, only those selected for an interview will be contacted.Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities.
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