CDISC jobs

Senior Statistical Programming Analyst - REMOTE ROLE

Remote

•

Today

Description: Location: Remote, all time zones welcome! Key Responsibilities: Develop and maintain SAS programs for clinical and real-world data analysis. Work with CDISC standards (SDTM, ADaM) experience is a major plus. Perform PASR reporting and/or IJ analysis as needed. Analyze real-world insurance files, registry data, and post-market trial registry datasets. Collaborate with CROs, Sponsors, and cross-functional teams to ensure data integrity and compliance. Deliver accurate, timely outputs

Easy Apply

Contract

$65 - $70

Veeva Clinical Database Programmer

Remote or Hybrid in Thousand Oaks, California

•

Today

Client: global biotech company Location:100% Remote from anywhere in the US Duration: 1 year + extensionsWe are seeking an experienced Veeva Clinical Database Programmer with strong expertise in clinical data standards to join our Biomedical Data Stewardship team. This role is responsible for contributing to the design of clinical trial databases within Veeva Clinical Data Management System (CDMS), ensuring compliance with internal data collection standards and supporting high-quality data entry

Easy Apply

Contract

BASED ON EXPERIENCE

Director of Data and Biostatistics (Only W2, No C2C)

Acton, Massachusetts

•

Today

Job Title: Director of Data and Biostatistics (Only W2, No C2C) Job Location: Acton, MA (Hybrid)Job ID: 407 Job Location: 12 Months Must be local to Acton, MA and available for onsite meetings Description: The Director of Data and Biostatistics will lead data operations for our Clinical Affairs team focused on medical devices. This role will be responsible for overseeing the design, implementation, and maintenance of clinical data systems, ensuring data integrity, and supporting regulatory co

Easy Apply

Contract

$130 - $145

Director of Data and Biostatistics

Acton, Massachusetts

•

Today

RESPONSIBILITIES: Kforce has a client in Acton, MA that is seeking a Director of Data and Biostatistics who will lead data operations for the Clinical Affairs team focused on medical devices. This role is responsible for overseeing the design, implementation, and maintenance of clinical data systems, ensuring data integrity, and supporting regulatory compliance across all clinical studies. Additionally, the Director of Data and Biostatistics will guide statistical analysis of clinical study data

Contract

$127 - $140 hourly

QA Specialist

Cambridge, Massachusetts

•

Today

We are seeking an experienced Quality Assurance (QA) Specialist with a strong background in clinical trials within the pharmaceutical industry. The ideal candidate will have hands-on experience ensuring data integrity and system compliance across clinical systems and cloud technologies. Key Responsibilities: Develop, document, and execute test plans, scenarios, and test cases for clinical trial applications and data workflows. Perform functional, regression, and integration testing to validate

Easy Apply

Contract, Third Party

$70 - $70 per hour

Director of Data and Biostatistics

Acton, Massachusetts

•

Today

Role:: Director of Data and Biostatistics Location :: Acton MA 01720 - 3 Days/Week Duration :: 12+ Months - Extension Possible Job Description: The Director of Data and Biostatistics will lead data operations for our Clinical Affairs team focused on medical devices. This role will be responsible for overseeing the design, implementation, and maintenance of clinical data systems, ensuring data integrity, and supporting regulatory compliance across all clinical studies. In addition, this role wil

Easy Apply

Contract

Director of Data and Biostatistics

Acton, Massachusetts

•

Today

Job DescriptionJob title: Director of Data and Biostatistics Location: Massachusetts The Director of Data and Biostatistics will lead all data and statistical functions within Clinical Affairs for medical device studies. This role oversees clinical data systems, ensures data accuracy and regulatory compliance, and directs statistical analysis to support safety, efficacy, and research objectives. Key Responsibilities: Lead data management strategy for medical device clinical trials. Support study

Full-time

Health IT Consultant

Remote

•

Yesterday

Vector Consulting is looking for an experienced Health IT Consultant on a remote 9+ months (part-time) renewable Government contract inSilver Spring, MD. Position:Health IT Consultant This individual will work across various clinical projects across the agency supporting the responsibilities below: Participating as a subject matter expert for any clinical safety studies, respectively, which are submitted to the agency in support of drug applications. Reviewing clinical data for regulatory comp

Easy Apply

Contract

Depends on Experience

Clinical Data Validation Engineer Specialist

Cambridge, Massachusetts

•

Today

100% Remote Objective / Purpose: As a Clinical Data Validation Engineer, you will work on Clinical Trial Reporting activities delivering listings and visualizations to support clients Clinical Trials. In addition, you will operate in compliance with clients SOPs and processes. Accountabilities: Create data cleaning reporting solutions with appropriate oversight that support the quality and timely delivery of data cleaning, study status metric, and monitoring reports and visualizations required

Easy Apply

Contract

Senior Programming Lead, Integrated Data Analytics and Reporting

Remote or Raritan, New Jersey

•

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 109,000.00 - 174,800.00 per year

Advisory, Data Scientist - CMC Data Products

Indianapolis, Indiana

•

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

Edison, New Jersey

•

Today

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all relevant deliverables including investigator brochures, publications, all regulatory submissions (

Full-time

Clinical SAS Programmer

Raleigh, North Carolina

•

Today

Responsibilities: Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes' SDTM Implementation Guide, project standards, and the study protocol. Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets. Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate. Provi

Full-time

Clinical SAS Programmer

Baltimore, Maryland

•

Today

Responsibilities: Perform data manipulation, analysis and reporting of primarily clinical trial data. Create SDTM data sets. Create analysis data sets. Program and generate tables, listings and graphs (TLGs). Validate and document SAS programs and output. Fulfil ad-hoc analysis requests. Other services as needed. Requirements: Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or related applicable field. Minimum of 5 to 8 ye

Full-time

Director, R&D Data Science, Data Products - Global Development

Remote or Hopewell Township, New Jersey

•

Today

Full-time

USD 161,000.00 - 276,000.00 per year

Clinical SAS Programmer

Omaha, Nebraska

•

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

Wilmington, Delaware

•

Today

Job Description: The Sr. SAS Programmer provides PKPD programming aspects of pharmacokinetics, pharmacodynamics data management by timely completion and high quality of all required deliverables. Responsibilities: Prepare data for state-of-the-art analysis, such as PPK, PKPD, exposure-response (efficacy or safety), and C-QTc, typically based on CDISC ADaM / SDTM datasets. Prepare data for state-of-the-art NCA analysis, such as ADPC, PP, and ADPP, including the creation of defined packages and r

Full-time

Clinical SAS Programmer

Austin, Texas

•

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 Engineering Lead

Cambridge, England

•

Today

Job Description Summary About the role: #LI:Onsite Are you ready to make a lasting impact by building the future of oncology research? Novartis Biomedical Research (NBR) is searching for a visionary Associate Director to lead Clinical Data Engineering within our Oncology Data Science (OncDS) team. In this pivotal role, you'll be at the forefront of shaping early clinical development by building innovative biomarker data infrastructure, championing translational research, unlocking AI-powered d

Full-time

USD 176,400.00 - 327,600.00 per year

SAS Programmer

New Jersey

•

Today

Responsibilities: You'll be at the forefront of developing and validating programs that create datasets conforming to CDISC standards. Your expertise will drive the creation of Tables, Listings, and Figures for analysis purposes. Depending on the complexity of the study, you may lead programming projects, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. You'll also have the opportunity to mentor junior programmers and represent Statistical Programming i

Full-time

Filter Results

Job post features

Posted date

Work settings

Employment type

Distance

Employer type

Work authorization