Statistical Programmer (Medical Device)

Washington, District of Columbia, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Medical Devices, Pharmaceuticals, BiotechnologyIndustries

Requirements

Candidates must possess a Master's degree in Computer Science or a related field with 3 years of relevant experience, or a Bachelor's degree in Computer Science or a related field with 4 years of relevant experience. Medical device experience and SAS certification are preferred. Strong knowledge of clinical research data standards, including CDISC SDTM, ADaM, and ICH Statistical Principles for Clinical Trials, is required. The role also demands advanced knowledge of computing applications like Base SAS, SAS Graph, and SAS Macro Language, along with good organizational, interpersonal, leadership, and communication skills. The ability to manage multiple tasks and projects effectively, coupled with excellent accuracy and attention to detail, is essential.

Responsibilities

The Statistical Programmer will provide technical expertise to develop process methodologies and coordinate the development of integrated programming solutions for statistical analysis. This includes programming, testing, and documenting statistical programs for tables, figures, and listings, as well as programming analysis databases and data transfers. Responsibilities also involve planning and coordinating the integration of databases from multiple sources, developing programming documentation, and providing advanced technical expertise to clients. The role includes independently solving complex project issues, developing, implementing, and validating new process technologies, and acting as a statistical team lead for studies. Additionally, the programmer will manage project scope, budget, and resource forecasts, and provide training and guidance to junior staff.

Skills

Statistical Programming

SAS

Data Analysis

Database Management

Programming

Testing

Documentation

Data Transfer

Quality Control

Project Management

Client Consulting

Process Development

Validation

Training

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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