CDISC jobs

Senior Director, Clinical Data Standards

Boston, Massachusetts

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Today

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Senior Director, Clinical Data Standard

Full-time

USD 208,200.00 - 327,140.00 per year

Statistical Programmer Consultant

Novato, California

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Today

A leading pharma company in California is seeking a new Statistical Programmer Consultant to provide programming support for clinical studies. this is a remote position. About the Opportunity: Shift: Day Schedule: Full-time Hours: 9am to 5pm Setting: Office/Lab Responsibilities: Providing programming support for multiple projects/studies across various therapeutic areas Creating and reviewing annotated CRF to SDTM datasets Balancing conflicting priorities and promoting effective communication Fu

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Contract

$76 - $76 per hour

Biostatistical Programmers

Piscataway, New Jersey

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Today

Headquartered in New Jersey, Rang Technologies has dedicated over a decade delivering innovative solutions and best talent to help businesses get the most out of the latest technologies in their digital transformation journey. Rang Technologies has grown to become a global leader in Analytics, Data Science, Artificial Intelligence, Machine Learning, Salesforce CRM, Cloud, DevOps, Internet of Things - IoT, Cybersecurity, IT Consulting and Staffing, and Corporate Training.Job title: Biostatistica

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Full-time

Clinical Programmer (Remote)

Bedford, Virginia

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Today

A pharma company has a great Remote opportunity awaiting a new Clinical Programmer, where they'll play a critical role in developing and validating SAS programs essential for data processes. About the Opportunity: Shift: Day Schedule: Full-Time Hours: 40 per week Setting: Remote Responsibilities: Developing and validating SAS programs for data review, cleaning, and reconciliation listings Programming listings, tables, profiles, figures, and datasets Executing existing SAS programs and debuggin

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Contract

$50 - $50 per hour

Sr. Biostatistician

Remote

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17d ago

Senior Biostatistician Location: Remote Contract Length: 6-month contract-to-hire Overview A clinical-stage pharmaceutical company has an immediate need for an experienced Senior Biostatistician to join its clinical development team. This role is an urgent backfill supporting a Phase clinical study and regulatory submission activities. The ideal candidate will bring strong sponsor-side clinical trial experience, preferably within ophthalmology, and be comfortable operating within a

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Contract, Third Party

Depends on Experience

Sr. Business Analyst with Clinical Trails _ 10+ Years Experience

Remote

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9d ago

Position:1 Position- Business Analyst with Clinical Trails Location- Remote Job Description: The Business Analyst (BA) will serve as a key liaison between clients, product teams, clinical operations, and technical delivery teams. The BA will gather, analyze, and translate complex clinical trial requirements into functional specifications for eSource, DDC, and eCOA solutions. This role requires strong understanding of clinical trial processes, data capture workflows, regulatory expectations (Go

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Contract

Depends on Experience

Clinical Data Management Technical Project Management Specialist

Remote or Philadelphia, Pennsylvania

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Today

The Clinical Data Management Technical Project Management Specialist is responsible for developing program/project plans and estimates and for end to end program/project management, scoping and requirements through implementation and deployment. The Clinical Data Management Technical Project Management Specialist proactively monitors and manages execution of deliverables. They serve as a single point of contact for the MACH1 client at a study level, accountable for predictable, timely, high qual

Full-time

USD 70,350.00 - 154,800.00 per year

Mgr Clinical Database Development

Tarrytown, New York

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Today

Manager, Clinical Database Development (Tarrytown, NY) Regeneron Pharmaceuticals, Inc. seeks a Manager, Clinical Database Development (Tarrytown, NY) to oversee the development and/or technical activities for EDC databases built by CRO partners for assigned studies. Ensure all database build activities are performed according to Regeneron Processes (or CRO processes where applicable). Contribute to the creation of CDASH compliant eCRFs. Maintain and contribute to company standard Global Library

Full-time

USD 142,958.00 - 184,700.00 per year

Manager, Data Science - Oncology

Remote or Pennsylvania

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

USD 117,000.00 - 201,250.00 per year

Data Standards Manager

South Plainfield, New Jersey

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Today

Roles and Responsibilities: eCRF Design - Able to critically review eCRF designs to ensure compatibility/conformance with CDASH/SDTM standards. Recognizes limitations in eCRF design and works with the study team to correct flaws proactively. SDTM Conformance Mapping - Create and Reviews SDTM conformance mapping specifications applying SDTM, TAUG and Client standard. CDISC Validation Tools - Executes validation tools (e.g., Pinnacle 21) and collaborates with other functions to resolve identified

Full-time

Associate Director, External Data Management

Remote or Warren, Ohio

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Today

The Associate Director, External Data Services, plays a critical leadership role, overseeing team members to ensure all activities align with Regeneron's procedures and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver structured external data in compliance with Regeneron SOPs. The role also involves coaching, mentoring, and managing the performance of direct reports, while contributing to the department's strateg

Full-time

USD 157,200.00 - 256,600.00 per year

Clinical SAS Programmer

Chicago, Illinois

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements Provides input in the design and development of case report forms and clinical databases Performs

Full-time

Sr. SAS Programmer

Remote or New Jersey

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Today

Job Description: The senior programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various data sources with a careful eye for outliers and errors. Prior experience building patient cohorts and evaluatin

Full-time

Clinical SAS Programmer

Jacksonville, Florida

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Today

Full-time

Clinical Data Specialist

Hartford, Connecticut

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Today

Responsibilities: Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing data capture forms and supplemental procedures to instruct the abstraction process You'll lead the execution of feasibility testing to de-risk data capture approaches, and own the implementation of data validation checks to ensure data quality In addition, you'll work alongside other team members on way

Full-time

Sr. Scientist, Statistical Programmer, Submission Data Standards Quality Management (Hybrid)

Remote or North Wales, Pennsylvania

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Today

Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities: The Senior Statistic

Full-time

USD 117,000.00 - 184,200.00 per year

Advisor, Data Scientist - CMC Data Products

Indianapolis, Indiana

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 126,000.00 - 244,200.00 per year

Clinical SAS Programmer

Boston, Massachusetts

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Perfo

Full-time

Clinical Data Specialist

Austin, Texas

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Today

Full-time

Clinical SAS Programmer

Omaha, Nebraska

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Today

Full-time

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