Junior Clinical Analyst Jobs

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Clinical SME Project Manager -AI/Gen AI knowledge

Apex 2000

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New York, New York, USA

Contract

Clinical SME Project Manager -AI/Gen AI knowledge Location: New York Duration: 9-12 month JD: Total Yrs. of Experience 10+ Relevant Yrs. of experience 10+ Mandatory skills Clinical R&D + Project management Comfortable working in a matrix environment with clinical, regulatory, and tech teams.Demonstrates strong problem-solving and decision-making under tight timelines.Ability to lead and coordinate cross-functional teams from offshore and onshore.Strong stakeholder management and communication
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Posted 6 days ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have hands-on phlebotomy experience and a strong background working within a clinical site network environment. This role is essential in supporting the execution of clinical trials across multiple therapeutic areas. Responsibilities for the Clinical Research Coordinator: Coordinate and manage day-to-day clinical trial activities in
Posted 39 days ago | Updated 28 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Lake Success, New York, 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 22 days ago | Updated 5 hours ago

Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.

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Remote

Contract

Job Title: Bidirectional Clinical Data Exchange Architect Location: Durham, NC (Remote) Project Duration: 6+ Months Contract (Only W2 Contracts) Job Description: The Bidirectional Clinical Data Exchange Architect will be responsible for designing, implementing, and maintaining bidirectional clinical data exchange solutions. This role requires a deep understanding of healthcare interoperability, data exchange standards, and clinical workflows. Key Responsibilities: Architecture Design: Design and
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Posted 48 days ago | Updated 10 hours ago

Clinical Data Specialist

Katalyst Healthcares and Lifesciences

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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 2 days ago | Updated 5 hours ago

Clinical Safety Coder - MedDRA/WHODrug

General Dynamics Information Technology

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Maryland, USA

Full-time

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: NACI (T1) Job Family: Medical Affairs Job Qualifications: Skills: Clinical Research, MedDRA, WHODrugCertifications: NoneExperience: 6 + years of related experienceship Required: Yes Job Description: GDIT's Military Health team is hiring a Clinical Safety Coder - MedDRA/WHODrug to support the Office of Regulated Activities (ORA) under the DoD (D
Posted 7 days ago | Updated 12 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Bridgewater, New Jersey, USA

Full-time

Responsibilities: Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users. Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design. Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implement
Posted 60+ days ago | Updated 5 hours ago

Clinical Research Associate

Zachary Piper Solutions, LLC

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Sacramento, California, USA

Full-time

Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Sacramento, California (CA). The Oncology Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monito
Posted 60+ days ago | Updated 28 days ago

Clinical Research Associate

Zachary Piper Solutions, LLC

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Los Angeles, California, USA

Full-time

Piper Companies is currently seeking a Clinical Research Associate (CRA) for an opportunity in Los Angeles, California (CA). The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation
Posted 60+ days ago | Updated 28 days ago

Clinical Field Service Engineer

Nityo Infotech Corporation

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Boston, Massachusetts, USA

Contract

Clinical Field Service Engineer Responsibilities: Conduct comprehensive inventory of clinical devices, including radiology modalities, as part of a network migration project to ensure accurate asset tracking and seamless integration into the new infrastructure.Update configuration settings on medical devices to ensure proper functionality and connectivity during a phased, site-by-site network migration.Respond to technical support requests and helpdesk tickets in a timely manner, ensuring resolu
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Posted 13 days ago | Updated 6 days ago

Clinical Data Lead - Vaccines

Sanofi U.S.

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Morristown, New Jersey, USA

Full-time

Job Title: Clinical Data Lead - Vaccines Location: Morristown, NJ About the Job The Clinical Data Lead adapts and coordinates the data management strategy during development and conduct of clinical studies/projects for the mRNA/vaccine team within Sanofi. In addition, the Clinical Data Lead ensures data integrity and quality for clinical studies in order to deliver a comprehensive clinical database, and contributes to the optimization of data management processes and innovations. We are an i
Posted 60+ days ago | Updated 4 hours ago

Clinical Data Analytics Leader

Software Guidance & Assistance

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South San Francisco, California, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Data Analytics Leader for a direct placement assignment with one of our premier Pharmaceutical Services clients in South San Francisco, CA. Responsibilities : The Data Analytics Leader (DAL) in Early Clinical Development (ECD) Data Intelligence team supports ECD study teams by delivering timely and high-quality analysis and real-time interactive visualizations. The DAL is an expert in data analysis and data insights, enabl
Posted 15 days ago | Updated 2 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal
Posted 60+ days ago | Updated 5 hours ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Indianapolis, Indiana, 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. Fulfil ad-hoc analysis requests. Provide other services. Requirements: Bachelor's deg
Posted 49 days ago | Updated 4 hours ago

Senior Consultant - Clinical Data Programming

Veeva Systems

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Raleigh, North Carolina, USA

Full-time

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation
Posted 60+ days ago | Updated 4 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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 3 days ago | Updated 5 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Irving, Texas, USA

Full-time

Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs). Production and QC / validation programming. Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP. Demonstrate good understanding of the endpoints and d
Posted 60+ days ago | Updated 5 hours ago

Senior Clinical Outcomes Assessment (COA) Lead

Sanofi

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Morristown, New Jersey, USA

Full-time

Job Title: Senior Clinical Outcomes Assessment (COA) Lead Location: Cambridge, MA, Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. The remit of the Clinical Outcome Assessment (COA) team at Sanofi is to incorporate the patients' perspective (and other subjective perspectives) into clinica
Posted 10 hours ago

Senior Clinical Outcomes Assessment (COA) Lead

Sanofi

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Cambridge, Massachusetts, USA

Full-time

Job Title: Senior Clinical Outcomes Assessment (COA) Lead Location: Cambridge, MA, Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. The remit of the Clinical Outcome Assessment (COA) team at Sanofi is to incorporate the patients' perspective (and other subjective perspectives) into clinica
Posted 10 hours ago

Clinical Business System Analyst - Healthcare, Trizetto Communication System

People Force Consulting Inc

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Remote

Contract

As an Clinical Business System Analyst, you will be a part of an Agile team to build healthcare applications and implement new features while adhering to the best coding development standards . Responsibilities: - Configuration Management Documentation: Create comprehensive documentation of configuration management processes.Develop process flowcharts for configuration management.Write step-by-step set-up and testing procedures.Prepare troubleshooting guides for common issues.Document version co
Easy Apply
Posted 60+ days ago | Updated 5 hours ago