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  • Posted: Mar 7, 2023
    Deadline: Not specified
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    IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...
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    Principal Statistical Programmer - Remote

    Responsibilities:

    • Import data from various sources
    • Program quality control checks for source data and reporting data issues
    • Interpret project level requirements and develop programming specifications
    • Write programming code following established Good Programming Practices
    • Program SDTM and ADaM datasets
    • Program to create statistical analysis tables, listing and figures
    • Validate datasets and all statistical outputs per prescribed gate checks
    • Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines
    • Use and promote the use of established standards, SOPs, and standard methodologies
    • Export data and clinical study report materials
    • Provide training and mentoring to team members and department staff

    You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas. Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and advanced statistical programming. Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.

    THE PERSON
    We know that meaningful results require not only the right approach, but also the right people. Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have a strong educational or practical evidence in programming.

    Key required skills include:

    • 3+ experience in Statistical Programmer role from CRO
    • Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication.
    • In light of the above, candidates for the roles should exhibit the following skills and competencies:
    • Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries
    • Knowledge of statistics and exhibit routine and occasionally complex analytical skills
    • A focus on quality, accuracy, and completeness of work activities
    • Excellent communication skills
    • A good understanding of Good Clinical Practice and ICH guidelines
    • Ability to independently lead (or have lead potential) and estimate programming scope of work, handle resource assignments, communicate work status, and work within project timelines for deliverables
    • Take initiative and can be counted on to get the job done, with integrity
    • Have the self-awareness to recognize when negotiating skills and assistance are needed
    • Ability to establish and maintain effective working relationships with co-workers, managers, and clients

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    Senior Statistical Programmer - Global BIOS

    Requirements:

    • Bachelors or Masters’ in Computer Science, Mathematics or equivalent
    • 5+ years Statistical Programming experience within the Life-Science industry
    • Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
    • Excellent knowledge of CDISC standards (SDTM and ADaM)
    • Excellent application development skills
    • Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
    • 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

    From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.

    What is in it for you?

    • Global exposure
    • Variety of therapeutic areas
    • Collaborative and supportive team environment
    • Access to cutting-edge in-house technology
    • Excellent career development and progression opportunities
    • Work-Life Balance

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    Senior Statistical Programmer: Real World Evidence

    Essential Requirements:

    • Already be an established Senior Statistical Programmer
    • 5+ years Statistical Programming experience within the Life-Science industry
    • Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
    • Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
    • Ability to implement more advanced statistical procedures as per specifications provided by Biostatisticians.
    • Excellent knowledge of CDISC standards (SDTM and ADaM)
    • Thorough understanding of relational database components and theory
    • Excellent application development skills
    • Bachelors or Masters’ in Computer Science, Mathematics or equivalent
    • In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
    • (GCP) and International Conference on Harmonization (ICH) guidelines

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    Senior Statistical Programmer: Patient Centered Endpoints

    Job Overview:

    As a Senior Statistical Programmer, you will provide experienced technical expertise and leadership to develop process methodology for the department to meet internal and external clients’ needs.

    You will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming. You will provide technical expertise and leadership to the department and provide internal consulting services such as specifications and user needs analysis for complex project or client requirements.

    Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. As well as estimating programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.

    Essential Requirements:

    • Already be an established Senior Statistical Programmer
    • 5+ years Statistical Programming experience within the Life-Science industry
    • Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
    • Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
    • Ability to implement more advanced statistical procedures as per specifications provided by Biostatisticians.
    • Excellent knowledge of CDISC standards (SDTM and ADaM)
    • Thorough understanding of relational database components and theory
    • Excellent application development skills
    • Bachelors or Masters’ in Computer Science, Mathematics or equivalent
    • In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
    • (GCP) and International Conference on Harmonization (ICH) guidelines

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    Statistical Programmer 2 - Real World Evidence

    Job Overview:

    • As a Statistical Programmer 2, you will provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.
    • You will plan and lead the development of project-related solutions to the full scope of statistical programming tasks.
    • As a lead programmer on assigned studies, you will write and maintain programming specifications datasets and program TLFs, to maximize programming efficiency with the use of biostatistical tools and assist in training and mentoring new or junior team members

    Essential Candidate Requirements:

    • Bachelors or Masters’ in Computer Science, Mathematics or equivalent
    • 3+ years, statistical programming experience within the Life Science industry in SAS
    • Experience as project lead, directly engaging clients and coordinating tasks within a programming team
    • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
    • Knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
    • Ability to independently lead multiple tasks and projects

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    Senior Consultant

    Job Overview

    Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales process.

    Essential Functions

    • Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects.
    • Reviews and analyzes client requirements or problems and assists in the development of proposals of cost effective solutions that ensure profitability and high client satisfaction.
    • Provides direction and guidance to Analysts, Consultants, and where relevant, to Statistical Services assigned to engagement.
    • Develops detailed documentation and specifications.
    • Performs qualitative and/or quantitative analyses to assist in the identification of client issues and the development of client specific solutions.
    • Designs, structures and delivers client reports and presentations that are appropriate to the characteristics or needs of the audience.
    • May deliver some findings to clients.
    • Recommends improvements and alternative solutions to resolve problems.
    • May identify new business opportunities of follow-on work and new leads at assigned client.
    • Provides follow-up with client after project deliverable has been completed to ensure client satisfaction.
    • Proactively develops broader and deeper knowledge of related consulting methodologies and life sciences market through on the job experience and participation in training opportunities. Begins to develop CoE specific subject matter expertise.
    • When acting as Project Manager, proactively manages project timelines and manages day to day communication with the client and team members.

    Qualifications

    • Bachelor's Degree Req
    • Master's Degree Business Administration Pref
    • 5-8 years of related experience in consulting and/or life sciences industry Req
    • Possesses solid project management skills and client influencing and relationship building skills.
    • Works willingly and effectively with others in and across the organization to accomplish team goals.
    • Experienced with developing consultative relationships with senior level managers and executives at clients in the life science industry.
    • Ability to manage multiple projects, juggle priorities and deliver on tight deadlines.
    • Knowledge of consulting methodologies, tools and techniques related to functional area.
    • Knowledge of key issues and current developments in the life science industry.
    • Excellent presentation, communication and client influencing skills.
    • Has established network and referral contacts.
    • Has necessary subject matter expertise to effectively manage projects within a given CoE.

    Method of Application

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