Jobs at IQVIA

RESPONSIBILITIES

• Provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. 
• Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. 
• Provide technical expertise and leadership to the department. 
• Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries
• Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
• In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of statistics, programming and/or clinical drug development process
• Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
• Good organizational, interpersonal, leadership and communication skills
• Ability to independently manage multiple tasks and projects
• Ability to delegate work to other members of the SP team
• Excellent accuracy and attention to detail
• Ability to delegate work to other members of the SP team [SPM]
• Exhibits routine and occasionally complex problem solving skills
• Recognizes when negotiating skills are needed and seeks assistance.
• Ability to lead teams and projects and capable of managing at a group level
• Ability to establish and maintain effective working relationships with co-workers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• Master’s degree in computer science or related field and 3 years relevant experience; Bachelor's degree or educational equivalent in computer science or related field and 5 years relevant experience; or equivalent combination of education, training and experience
• Previous experience at a Clinical Research Organization highly beneficial

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RESPONSIBILITIES

• Develop analysis plans, table shells, programming and table specifications; produce tables, listings and figures; perform data review and statistical analysis.
• Assist with protocol development, sample size calculation, protocol and case report form (CRF) review.
• Advise data management staff on database design, and critical data. May advise on validation checks.
• Write statistical sections of integrated reports.
• Under supervision, act as statistical team lead for single studies.
• Understand the Scope of Work, budget and quote assumptions, estimate the work completed, and manage scope for single studies. May manage project budget and resource requirements and provide revenue and resource forecasts for single studies.
• Assist with review of RFPs and QIPs; prepare proposal text. May participate in bid defense meetings.
• Provide training and guidance to lower level and new staff.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Excellent written and oral communication skills including grammatical/technical writing skills
• Excellent attention and accuracy with details
• In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trials
• Strong individual initiative
• Strong organizing skills
• Strong working knowledge of SAS computing package
• Familiarity with other relevant statistical computing packages such as StatXact
• Strong commitment to quality
• Ability to effectively manage multiple tasks and projects
• Ability to provide and accept direction of lead team members
• Ability to solve moderately complex problems
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• Working knowledge of relevant Data Standards (such as CDISC/ADaM)

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• B Sc Degree in Biostatistics or related field and 3 years prior relevant experience.
• Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.