Stat Programmer 2 at IQVIA

Bengaluru, Karnataka, India

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Clinical ResearchIndustries

Requirements

Minimum 5 years of core SDTM programming experience
Equivalent combination of education, training, and experience
Knowledge of statistics, programming, and/or clinical drug development process
Working knowledge of computing applications such as Base SAS, SAS/STAT, and SAS Macro Language
Good organizational, interpersonal, leadership, and communication skills
Master's Degree in Computer Science or related field (preferred)
Bachelor's Degree in Computer Science or related field
Ability to effectively handle multiple tasks and projects
Excellent accuracy and attention to detail
Ability to establish and maintain effective working relationships with coworkers, managers, and clients

Responsibilities

Provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs
Plan and lead the development of project-related solutions to the full scope of statistical programming tasks
Provide technical expertise to the Statistical Programming department
Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures, and listing summaries, (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
Program the integration of databases from multiple studies or sources
Develop programming documentation including plans and specifications, as appropriate
Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department
Perform and plan the development, implementation, and validation of new process technologies, macros, and applications
Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision
Understand the Scope of Work, estimate the work completed, and manage Out of Scope for single studies. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions
Provide training and guidance to lower level and new staff

Skills

Key technologies and capabilities for this role

SDTMSASBase SASSAS/STATSAS Macro LanguageStatistical ProgrammingTFLAnalysis DatasetsMacros

Questions & Answers

Common questions about this position

What experience is required for this Stat Programmer 2 role?

A minimum of 5 years of core SDTM programming experience is required, along with knowledge of statistics, programming, and clinical drug development processes.

What technical skills are needed for this position?

Working knowledge of Base SAS, SAS/STAT, and SAS Macro Language is required.

What are the educational qualifications for this job?

A Master's or Bachelor's Degree in Computer Science or a related field is required.

What soft skills are important for this role?

Good organizational, interpersonal, leadership, and communication skills are needed, along with the ability to handle multiple tasks, maintain accuracy, and build effective working relationships.

What does IQVIA do as a company?

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries, focusing on accelerating medical treatments to improve patient outcomes.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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