Clinical trials Jobs

Refine Results
61 - 80 of 175 Jobs

Senior Specialist, Translational Immunology Data Science

Merck & Company Inc

•

San Diego, California, USA

Full-time

Job Description The Data, AI, and Genome Sciences (DAGS) department at our company is seeking a highly motivated and skilled data scientist to join our Translational Immunology Analytics team based in San Diego, CA. This individual will play a crucial role in analyzing and interpreting complex multi-omics datasets in immune-mediated diseases generated using various high-throughput platforms. The ideal candidate will possess a deep understanding of computational biology, statistical methods, AI/
Posted 26 days ago | Updated 8 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Newark, New Jersey, USA

Full-time

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.
Posted 4 days ago | Updated 8 hours ago

Sr. Systems and Hardware Engineer

Analog Devices, Inc.

•

Wilmington, Massachusetts, USA

Full-time

About Analog Devices Analog Devices, Inc. (NASDAQ: ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world. With revenue of more than $9 billion in FY24 and approximately 24,000 people globally, ADI
Posted 60+ days ago | Updated 8 hours ago

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

•

Durham, North Carolina, USA

Full-time

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming support i
Posted 10 days ago | Updated 8 hours ago

Agentic AI Engineering Lead

Eli Lilly and Company

•

Indianapolis, Indiana, USA

Full-time

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
Posted 60+ days ago | Updated 8 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Minneapolis, Minnesota, USA

Full-time

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.
Posted 7 days ago | Updated 8 hours ago

Linux Platform Operations Engineer

Eli Lilly and Company

•

Indianapolis, Indiana, USA

Full-time

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
Posted 60+ days ago | Updated 8 hours ago

Sr. Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Newark, New Jersey, USA

Full-time

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and ADaM specifications. Create and validate SDTM data sets. Create and validate analysis data sets. Create and validate patient profiles. Program and generate tables, figures, and listings (TFLs). Validate and document SAS programs and outputs. Fulfill ad-hoc analysis requests. Provide other services. Requirements: Ba
Posted 14 days ago | Updated 8 hours ago

Data Scientist

Novartis

•

Cambridge, England, United Kingdom

Full-time

Job Description Summary The Multimodal Data and Analytics group in Advanced Quantitative Sciences, Novartis Development is searching for a Data Scientist to support the design and hands-on execution of modeling strategies using patient-level -omics, imaging and clinical outcomes data. As part of interdisciplinary drug development teams, your work will influence development decisions and inform late phase trials and regulatory submissions. Your focus will be on combining your domain knowledge of
Posted 60+ days ago | Updated 8 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Omaha, Nebraska, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 13 days ago | Updated 8 hours ago

Prin Clin Data Scientist (Data Mgr)

Novartis

•

Hanover

Full-time

Job Description Summary Location: East Hanover, NJ Onsite (cannot be done remotely) Hiring for multiple roles. About the role: Love clinical data management? Bring that passion to Novartis! This key Principal Clinical Data Scientist will be responsible and accountable for managing all Data Management deliverables at a consistently high standard with respect to cost, quality, and timelines for all assigned indications within one or more Global Clinical Program(s)/Project(s). Job Description
Posted 60+ days ago | Updated 8 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Dallas, Texas, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 18 days ago | Updated 8 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Princeton, New Jersey, USA

Full-time

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.
Posted 19 days ago | Updated 8 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Athens, Georgia, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 27 days ago | Updated 8 hours ago

Senior Data Architect

McKesson Corporation

•

Tennessee, USA

Full-time

It's More Than a Career, It's a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives
Posted 19 days ago | Updated 8 hours ago

Clinical Data Specialist

Katalyst Healthcares and Lifesciences

•

Alameda, California, USA

Full-time

Job Description: This position will play a critical role in ensuring the ethical and responsible conduct of clinical trials to protect study participants from potential harm, safeguard the integrity of the trial. By identifying potential problems early, the clinical data specialist can help prevent serious adverse events and ensure that the trial results are reliable and informative. Perform responsibilities meeting project commitments and in compliance with applicable regulations, good clinica
Posted 5 days ago | Updated 8 hours ago

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

•

Seattle, Washington, USA

Full-time

Responsibilities: The Senior SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming suppor
Posted 11 days ago | Updated 8 hours ago

Process Analytical Technology Strategy Leader Lilly Medicine Foundry

Eli Lilly and Company

•

Indianapolis, Indiana, USA

Full-time

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
Posted 4 days ago | Updated 8 hours ago

Clinical Data Specialist

Katalyst Healthcares and Lifesciences

•

Illinois, USA

Full-time

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
Posted 18 days ago | Updated 8 hours ago

Director, IT PMO (BLS)

LabCorp

•

Durham, North Carolina, USA

Full-time

Labcorp's Corporate IT is actively searching for an experienced Director, IT Project Management, Biopharma Laboratory Services, who will leverage their technology and project delivery skills to ensure IT programs and projects meet organizational goals. As a strategic leader, you will direct project management staff and partner with other department leaders to define, prioritize, develop, and implement projects and programs. You will be accountable for directly managing one or two programs and en
Posted 16 days ago | Updated 8 hours ago