Urwah Admin

IQVIA

<div><p><b>Job Overview</b><br>
With oversight at a team/site/staff level, lead complex studies and submissions. Develop protocols, review case report forms (CRFs), and develop analysis plans. Provide input or write specifications for tables and analysis files. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Interpret analyses and write statistical sections of study reports. Accountable for controlling costs and maximizing revenue recognition.</p><p></p><div><b>
Essential Functions</b><br>
<ul><li>Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Oversees team with same expectations. Prioritizes and works proactively to gain efficiency.</li><li>Leadership: Perform as lead statistician on complex studies and for integrated summaries or eSubmissions, where applicable. Through this, works with the team to ensure high quality deliverables, delivers on time within budget, ensures compliance with Standard Operating Procedures (SOPs), ensure consistency across teams and across protocols, manages/delegates data quality issue resolutions. As a lead of groups of studies within a compound, also prioritizes and leads proactively to gain efficiencies in work across protocols. Responsible for driving statistical discussions, actively participates in internal project team meetings, provides timely progress updates. If in lead role, runs meetings, provides timeline updates, assess resource needs, and documents and follows up on actions. Supports colleagues and provides motivation.</li><li>Datasets: Writes and maintains programming specifications, with a focus on efficacy. Manages dataset derivations and assignment. May program analysis datasets, including complex domains and derivations. Handles analysis set derivations and assignment.</li><li>Tables, Listings and Figures (TLFs): Writes programming specifications for statistical analyses outputs. Checks outputs for format and content. Ensures consistency across items produced. May program complex Tables/Figures (Main or QC), using Bios tools where applicable.</li><li>Timelines: Plans, documents, and negotiates timelines forecasts resource needs, identifies out of scope work.</li><li>Customer: Serves as primary point of contact for customer. Responsible for building and maintaining effective client relationships, providing direction, support and oversight of statistical activities. Consults on operational topics with clients as well as on statistical/programming topics, regardless of complexity. Provide best in class solutions. Act as oversight on any study, regardless of complexity. May oversee programs of studies or relationships.</li><li>Knowledge Sharing: Helps train staff regarding operational and technical items. Provides new topics and training materials at a department/site/ team/Global level. May be expected to act as subject matter expert (SME) to mentor senior staff, including offshore. Expected to mentor staff to contribute to conferences, as well as society/university involvement. May be contributing to the advertisement of IQVIA Biostatistics (e.g. meeting with clients there) and connecting with thought leaders.</li><li>Risk Management: Identifies risks to project delivery and/or quality, leads in a way that risks are avoided. Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions. Handles most study level escalations that do not impact the account relationship and escalates for support to business segment owners/client owners/managers.</li><li>Lock and Unblinding Process: Leads the database lock and unblinding process. May participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules). Serves as unblinded lead statistician in addition to overseeing lower level Bios new to unblindings. May attend DMCs.</li><li>Statistical Expertise: Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures and statistical sections for complex and/or integrated reports). Provide expert input into data management deliverables (i.e. database design, validation checks and critical data). Perform senior biostatistician review (SBR). Produce or perform quality control review of sample size calculations for complex studies.</li><li>Financials: Shares accountability (with resource managers) for the financial success of assigned studies. Accountable for controlling costs and maximizing revenue recognition. Also responsible for sharing budget expectations with the team. Responsible for negotiating out of scope work. Understands 'scope of work', contract, and budget assumptions. Project leads collaborate on creation/revisions of Estimate at Completion (EAC) reporting.</li><li>Proposals: Able to review and comment on proposals/budgets at a study level. May contribute to request for proposals (RFP) as well as full service proposals. Expected to present at bid defenses and contribute to FSP bids.</li><li>Other Responsibilities: As defined on ad-hoc basis by senior managers. May assist with cross functional collaboration.</li></ul></div><p></p><div><b>
Qualifications</b><br>
<ul><li>Bachelor's Degree Biostatistics or related field and 5 - 7 years relevant experience Req</li><li>Master's Degree Biostatistics or related field and 5-7 years relevant experience Pref</li><li>Typically requires 5 - 7 years of prior relevant experience, or equivalent combination of education, training and experience.</li><li>Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.</li><li>Excellent written and oral communication skills including grammatical/technical writing skills.</li><li>Excellent attention and accuracy with details.</li><li>In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li><li>Familiarity with moderately complex statistical methods that apply to applicable clinical trials.</li><li>Strong individual initiative.</li><li>Strong organizing skills.</li><li>Strong working knowledge of SAS computing package.</li><li>Familiarity with other relevant statistical computing packages such as nQuery.</li><li>Strong commitment to quality.</li><li>Ability to effectively manage multiple tasks and projects.</li><li>Ability to lead and co-ordinate small teams.</li><li>Ability to solve moderately complex problems.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Expert knowledge of relevant Data Standards (such as CDISC/ADaM)</li></ul></div><p></p><p>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</p><p></p><p>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</p><p></p>
The potential base pay range for this role, when annualized, is $96,400.00 - $241,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div>

Statistical Scientist - FSP

<div><p>Job Overview<br>
Provide experienced technical expertise to develop process methodology for department to meet internal and external clients&rsquo; 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.</p><div>
Essential Functions<br>
<ul><li>Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.</li><li>Program and plan the integration of databases from multiple studies or sources.</li><li>Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.</li><li>Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.</li><li>Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.</li><li>Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies.</li><li>Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.</li><li>Provide training and guidance to lower level staff.</li></ul></div><div>
Qualifications<br>
<ul><li>Master's Degree Computer science or related field and 11 years relevant experience Req Or</li><li>Bachelor's Degree Computer science or related field and 12 years relevant experience Req</li><li>Equivalent combination of education, training and experience in lieu of degree Req</li><li>Knowledge of statistics, programming and/or clinical drug development process</li><li>Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language</li><li>Good organizational, interpersonal, leadership and communication skills</li><li>Ability to effectively manage multiple tasks and projects</li><li>Excellent accuracy and attention to detail</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients</li></ul></div><p></p><p>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</p></div>

Stat Programmer Scientist

<div><p>Job Overview
<br>
Provide experienced technical expertise to develop process methodology for department to meet internal and external clients&rsquo; 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.
</p><div>Essential Functions
<br>
<ul><li>Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.
</li><li>Program and plan the integration of databases from multiple studies or sources.
</li><li>Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
</li><li>Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.
</li><li>Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.
</li><li>Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies.
</li><li>Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.
</li><li>Provide training and guidance to lower level staff.
</li></ul></div><div>Qualifications
<br>
<ul><li>Master's Degree Computer science or related field and 11 years relevant experience Req Or
</li><li>Bachelor's Degree Computer science or related field and 12 years relevant experience Req
</li><li>Equivalent combination of education, training and experience in lieu of degree Req
</li><li>Knowledge of statistics, programming and/or clinical drug development process
</li><li>Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language
</li><li>Good organizational, interpersonal, leadership and communication skills
</li><li>Ability to effectively manage multiple tasks and projects
</li><li>Excellent accuracy and attention to detail
</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients
</li></ul></div><p></p><p>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com</p></div>

<div><p><b>Job Description Summary</b></p><p>
This position supports IQVIA&rsquo;s new MedTech business intelligence tool that gives insights into the orthopedic market at a procedure level. The role is responsible for supporting, scaling, and enhancing the product and being the lead consultant for client support.<br>
IQVIA is looking for a Sr. Consultant in the MedTech domain. This role will be collaborating with a team of product owners, associate directors, product offering managers, and client service professionals on a data delivery team. This position will work between internal teams and clients to ensure successful implementation, understanding, and usage of the product.</p><p></p><p>
This role will also oversee a small team responsible for other newly launched offerings ensuring operational continuity. The position will lead through direct team meetings, 1:1s, ad hoc support, and ensuring project oversight for new initiatives. The individual will drive cross-functional initiatives that span client success, product delivery, and internal process optimization, including development and refinement of new SOPs and workflows.</p><p></p><p><b>
Responsibilities</b>:</p><ul><li>
Implement and support clients on a platform for procedure level data &amp; market growth</li><li>
Collaborate directly with clients to understand their needs and gather requirements</li><li>
Provide recommendations to clients on approaches to derive data insights</li><li>
Collaborate with internal teams to support the creation and enhancements surrounding a new product(s)</li><li>
Assist in the QC process and sign off before new data and enhancements are pushed to the production environment.</li><li>
Draft and distribute quarterly product information bulletins informing clients of changes/updates to the data and tool itself.</li><li>
Create, evaluate, and manage documentation between clients and IQVIA to align on requirements and expectations for successful platform usage</li><li>
Train clients on platform usage&mdash;including assisting in developing clear &amp; effective client training materials</li><li>
Track and maintain reports on client usage of platform.</li><li>
Manage offshore resources in the development of insights presentation by holding meetings, establishing a feedback loop, and ensuring a robust QC process onshore before decks are ready for client distribution.</li><li>
Manage process flows and workstreams</li><li>
Work towards the highest standards of client service &amp; engagement management best practices</li><li>
Provide subject matter expertise to client stakeholders and internal IQVIA team regarding data &amp; platform usage</li><li>
Serve as the escalation point for unresolved data issues, work with client data managers &amp; internal team members for resolution</li><li>
Establish strong communications with internal team, client contacts, and all other stakeholders</li><li>
Proactively continue to strengthen subject matter expertise through on the job experience</li><li>
Openness to learning about innovative technologies and acquiring new skills</li><li>
Manage a team of client service professionals, providing direction and guidance and developmental opportunities.</li><li>
Ensure team oversight for new and cross-functional initiatives to develop and scale new processes as offerings grow and expand.</li></ul><p><b><br>
Qualifications</b>:</p><ul><li>
5-8 years of related experience in consulting and/or life sciences industry Req; experience in Med Tech area preferred</li><li>
Prior management experience preferred</li><li>
Possesses solid project management skills and client influencing and relationship building skills.</li><li>
Works willingly and effectively with others in and across the organization to accomplish team goals.</li><li>
Experienced with developing consultative relationships with senior level managers and executives at clients in the life science industry.</li><li>
Ability to manage multiple projects, juggle priorities and deliver on tight deadlines.</li><li>
Knowledge of consulting methodologies, tools and techniques related to functional area.</li><li>
Knowledge of key issues and current developments in the life science industry.</li><li>
Excellent presentation, communication, and client influencing skills.</li><li>
Has necessary subject matter expertise to effectively manage projects within a given Center of Excellence</li></ul><p></p><p>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</p><p></p><p>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</p><p></p>
The potential base pay range for this role, when annualized, is $95,300.00 - $237,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div>

Sr. Consultant - MedTech

<div><p><b>Job Overview</b><br>
Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports. Accountable for controlling costs and maximizing revenue recognition. Provide training, guidance and mentorship to lower level and new staff.</p><p></p><div><b>
Essential Functions</b><br>
<ul><li>Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Conducts all appropriate validation requirements, according to Standard Operating Procedures (SOPs), for each task undertaken. Checks programming logs for cleanliness and correct processing of data. Inputs into Data Issues log and follows issues to appropriate resolution.</li><li>Leadership: Perform statistical team lead role on single studies. Through this, works closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget. Build and maintain effective customer relationships, driving statistical discussions, providing support and/or guidance for statistical activities. Demonstrates and promotes efficient communication. If in lead role, runs meetings, documenting where necessary and following up on actions. Actively participates in internal project team meetings, provides timely progress updates. As a lead, will have input on estimate at completion (EAC) reporting.</li><li>Data Management: Assist in reviewing or advising data management staff on database design, validation checks and critical data. Handles data issue resolutions. If in lead biostatistical role, handles lock and unblinding process with appropriate supervision.</li><li>Statistical Analysis Plan (SAP) and Shells: Authors or performs quality control review (QC) of SAPs and shells. Make best use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods). May author or QC complex SAPs, under supervision if needed.</li><li>Datasets: Writes and maintains programming specifications. Programs assigned datasets to industry standards. Handles dataset derivations and assignment.</li><li>Tables, Listings and Figures (TLFs): Writes programming specifications for statistical analyses outputs. Programs TLFs, maximizes programming efficiency with use of tools, where applicable. Checks resulting output for format and content, and questions specification as needed. Ensures consistency across items produced.</li><li>Timelines: Plans and documents timelines, forecasts resource needs, suggests work may be out of scope.</li><li>Financials: Shares accountability (with resource managers) for the financial success of assigned studies. Accountable for controlling costs and maximizing revenue recognition. Responsible for sharing budget expectations with the team. Raises concerns to manager if new work or rework appears to be out of scope. Understands 'scope of work' and has an awareness of contract and budget assumptions.</li><li>Knowledge Sharing: Helps train staff regarding operational items. Mentors junior staff. Supports colleagues and provides motivation as needed.</li><li>Risk Management: Identifies risks to project delivery and/or quality and spends time to proactively avoid as well as proposes solutions to mitigate risks. Where possible, anticipate risks to minimize need for study level escalations.</li><li>Other Clinical Data Interchange Standards Consortium (CDISC) requirements: Leadership: Under supervision within Compound. May perform statistical team lead role on studies within a compound. In addition to the leadership responsibilities above, also prioritizes and takes proactive approach to gain efficiencies in work across protocols.</li><li>Study Start up: Assist with protocol development, sample size calculation, protocol and case report form (CRF) review.</li><li>Protocol: Authors or performs quality control (QC) review of the statistical section of a protocol (making best possible use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods).</li><li>Proposals: May be able to review and comment on proposals/budgets at a study level. May contribute to request for proposals (RFP). May be expected to present at bid defenses.</li><li>Clinical Study Report (CSR): Reviews or drafts CSR or statistical report.</li><li>Customer: On occasion, may serve as primary point of contact for customer. May also consult on operational topics with clients.</li><li>Lock and Unblinding Process: Handles the database lock and unblinding process. May participate on the biostatistics randomization team (drafts randomization specifications and/or reduce or perform quality control (QC) review of randomization schedules). May serve as unblinded lead statistician.</li><li>Other Responsibilities: As defined on ad-hoc basis by managers. May assist with cross functional collaboration.</li></ul></div><p></p><div><b>
Qualifications</b><br>
<ul><li>Bachelor's Degree Biostatistics or related field and 3 - 5 years relevant experience Req Or</li><li>Master's Degree Biostatistics or related field and 3-5 years relevant experience Req Or</li><li>Ph.D. Biostatistics or related field and 1 year relevant experience Req</li><li>Typically requires 3-5 years of prior relevant experience, or equivalent combination of education, training and experience.</li><li>Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.</li><li>Excellent written and oral communication skills including grammatical/technical writing skills.</li><li>Excellent attention and accuracy with details.</li><li>In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li><li>Familiarity with moderately complex statistical methods that apply to applicable clinical trials.</li><li>Strong individual initiative.</li><li>Strong organizing skills.</li><li>Strong working knowledge of SAS computing package.</li><li>Familiarity with other relevant statistical computing packages such as nQuery.</li><li>Strong commitment to quality.</li><li>Ability to effectively manage multiple tasks and projects.</li><li>Ability to lead and co-ordinate small teams.</li><li>Ability to solve moderately complex problems.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium CDISC/ADaM).</li></ul></div><p></p><p>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</p><p></p><p>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</p><p></p>
The potential base pay range for this role, when annualized, is $96,400.00 - $241,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div>

Sr. Clinical Bioinformatics Data Scientist - FSP

<div><div>Job Overview
<br>
Under general supervision, provides systems support in developing and enhancing business systems to provide new or enhanced products to clients or effective planning, reporting, and analysis tools to internal functions.
<br>
<br>
Essential Functions
<br>
<ul><li>Formulates and defines systems scope and objectives through research and fact-finding combined with an understanding of applicable business systems and requirements.
</li><li>Develops or modifies moderately complex information systems.
</li><li>Includes analysis of business and user needs, documenting requirements, and revising existing system logic difficulties as necessary.
</li><li>Guides and advises less-experienced Business Systems Analysts.
</li><li>Competent to work in some phases of systems analysis and considers the business implications of the application of technology to the current business environment.
</li><li>Is able to understand and analyze Lab Data - to then present back to stakeholders
</li><li>Will use PowerBI to create functional working product prototypes to aid solutioning and requirements elicitation
</li><li>Querying Systems Data using SQL
</li><li>Will coordinate and drive a Project from concept through to finalization, under general supervision
</li></ul><br>
Qualifications
<br>
<ul><li>Bachelor's Degree Computer Science or Life Sciences, or equivalent experience
</li><li>Six (6) years experience in IT within a Lab setting. Preferable: Three (3) years experience as a Business Analyst within Lab/Clinical Trials setting
</li><li>Knowledge of business-wide applications (e.g. third party software internal operational applications, etc.) or IQVIA client facing applications and products
</li><li>Demonstrated ability to understand client requirements and as well as underlying infrastructure applications, systems and processes to enable execution of those skills.
</li><li>Thorough knowledge of IQVIA data and current systems.
</li><li>Ability to query data using SQL
</li><li>Knowledge and ability to use PowerBI to effectively present analytical data
</li></ul></div><p></p><p>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com</p></div>

Sr Business Systems Analyst

<div><p>Job Overview<br>
Designs/develops software solutions requiring general domain knowledge and developing business experience.<br>
Analyzes user requirements/needs and makes decisions within limited parameters under regular supervision.</p><div>
Essential Functions<br>
<ul><li>Designs/develops software solutions requiring general domain knowledge and specialized business experience.</li><li>Works at all layers of the application stack including front-end user interface and backend development.</li><li>Analyzes user requirements/needs and makes decisions within general parameters under regular supervision.</li><li>Supports and often lead projects within own organization with limited complexity, including the development of medium size system components.</li><li>Has strong and broad understanding of quality standards and work requires minimal revision.</li><li>Reviews complex functional specifications and other validation deliverables as assigned.</li><li>Provides peer support and helps on-board new Software Engineers to the team.</li></ul></div><div>
Qualifications<br>
<ul><li>Bachelor's Degree Computer Science, a related field, or equivalent experience</li></ul>
 Req Or<br>
<ul><li>3 to 5 years prior related experience in developing web applications, graduate experience, or demonstrated success in development with DrugDev Spark or equivalent system Req</li><li>Experience with Ruby on Rails, Python, React, Ember or similar web framework.</li><li>Ability to write clean code</li><li>History of successfully designing small to medium system components</li><li>Good interpersonal communication and presentation skills</li><li>Attention to detail</li><li>Technical/functional expertise</li><li>Communication</li><li>Decision making</li><li>Customer focus</li><li>Conflict management</li><li>Energy, motivation and work rate</li></ul></div><p></p><p>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</p></div>

Software Development Engineer 4

Join IQVIA and explore 38   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

IQVIA

ABOUT_COMPANY

Statistical Scientist - FSP

Stat Programmer Scientist

Stat Programmer Scientist

Sr. Consultant - MedTech

Sr. Clinical Bioinformatics Data Scientist - FSP

Sr Business Systems Analyst

Software Development Engineer 4