clinical trial manager Jobs

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Clinical Documentation SpecialistCDIin California

Pyramid Consulting, Inc.

Remote

Contract

Immediate need for a talented Clinical Documentation Specialist CDI in California. This is a 06+months contract opportunity with long-term potential and is located in California(REMOTE). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-77657 Pay Range: $45 - $50/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Effec

Clinical Project Manager

Info Way Solutions

New York, New York, USA

Contract, Third Party

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 across time zones and geographies.Proactively identify opportunities for process automationSkilled at translating business needs into technical project requirements.Ability t

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

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

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

Eyecare Clinical Systems Engineer

Sunrise Systems, Inc.

Remote

Contract

Our client, a leading vision care insurance company, is looking for an Eyecare Clinical Systems Engineer. This is for an initial duration of 5 months and is fully remote. Must Haves: This person will work with Ventures teams to understand clinical hardware at the sites, installation and configuration of equipment.Must have clinical experience in Eyecare and eye equipment (eye exam)Need to have Clinical Application function with clinical devices.Must understand data traffic.Able to configure and

Clinical Research Engineer

OSI Engineering, Inc.

Mountain View, California, USA

Full-time

A global device company is looking for a Clinical Research Engineer to join its innovative team focused on advancing digital health technologies. In this role, you will collaborate closely with clinical scientists and cross-functional teams to design, execute, and monitor clinical studies, with a focus on biosensor data quality and analysis. The ideal candidate will have experience with clinical datasets, wearable health sensors, cloud data solutions like AWS, and familiarity with regulatory sta

Clinical Research Associate

OSI Engineering, Inc.

Mountain View, California, USA

Full-time

A global device company is looking for a motivated Clinical Research Associate to support studies involving wearable sensor technology and human subject data collection. Key responsibilities include executing data-collection protocols, preparing devices, coordinating study logistics, and ensuring high-quality data. If you have a background in engineering or a related field, experience with mobile sensors or wearables, and a passion for advancing health technology, we invite you to apply and joi

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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Boulder, Colorado, 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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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

Clinical Business/Data Analyst - NYC (onsite)

Winston Staffing Service

New York, New York, USA

Contract

This position requires onsite, 5 days a week, Monday Friday in Downtown, NYC. This Role will be 100% on site with potential to hire. If hired, it will be 2 days at home and 3 days in office. Interviews will be Virtual and only PREA required. Previous experience working with Clinical Data a must **NO AGENCIES, NO EMPLOYERS, NO 1099, NO C2C Must have year of experience gathering and documenting business, clinical, and/or functional requirements for software applications development and implement

Clinical Editing Coding Analyst | Remote | Contract

Walker Healthforce

Remote

Contract

Clinical Editing Coding Analyst |Remote |Contract Walker Healthforce is seeking a Clinical Editing Coding Analyst with 1-5+ years of experience.. This is a 6-month contract opportunity. CORE REQUIREMENTS: Certified Professional Codercertification (e.g., CPC, CCS, CCS-P, or RHIT) 1-5 years experience - in billing/coding (preferably in a comprehensive surgical center or facility) or Claims resolution (including adjudication, coding, thorough analysis and problem-solving) Ability to analyze, inves

Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.

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

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

Clinical Field Service Engineer

Nityo Infotech Corporation

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

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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

Clinical Data Analytics Leader

Software Guidance & Assistance

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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Cambridge, Massachusetts, USA

Full-time

Responsibilities: Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal al study data as tables, listings, and graphs for electronic submission to regulatory agencies. Attending multi-disciplinary team meetings, representing the programmi