Clinical Trial Manager Jobs

21 - 40 of 124 Jobs

Clinical Research CoordinatorJob Title - Clinical Research Coordinator

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a highly organized and proactive Clinical Research Coordinator (CRC) to support clinical trials across multiple therapeutic areas on-site in the Raleigh, NC area. This role is essential in ensuring smooth trial execution within a clinical site network, with a focus on phlebotomy and patient coordination. Key Responsibilities of the Clinical Research Coordinator: Oversee day-to-day clinical trial activities while ensuring compliance with Google Cloud Platform, IRB, and

Clinical Project ManagerJob Title - Clinical Project Manager

Info Way SolutionsCompany Name - Info Way Solutions

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New York, New York, USA

Third Party, Contract

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 Research CoordinatorJob Title - Clinical Research Coordinator

Zachary Piper Solutions, LLCCompany Name - 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

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

Senior Clinical Java ArchitectJob Title - Senior Clinical Java Architect

TrorCompany Name - Tror

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Eden Prairie, Minnesota, USA

Third Party, Contract

Position: Senior Clinical Java Architect Location: Eden Prairie, Minnesota (Hybrid 3 days onsite) Duration: 6+ months Contract: C2C/w2 Job Description: Seeking a highly experienced Clinical Java Architect with a strong background in designing and implementing complex, high-availability clinical systems in healthcare settings. This role demands deep expertise in Java-based backend architectures, along with hands-on knowledge of healthcare data standards (e.g., HL7, FHIR, CCD, DICOM) and int

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Athens, Georgia, USA

Full-time

Eyecare Clinical Systems EngineerJob Title - Eyecare Clinical Systems Engineer

Sunrise Systems, Inc.Company Name - Sunrise Systems, Inc.

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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 AssociateJob Title - Clinical Research Associate

OSI Engineering, Inc.Company Name - OSI Engineering, Inc.

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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 SpecialistJob Title - Clinical Data Specialist

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Boulder, Colorado, USA

Full-time

Clinical SME Project Manager -AI/Gen AI knowledgeJob Title - Clinical SME Project Manager -AI/Gen AI knowledge

Apex 2000Company Name - 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

Clinical Data AssociateJob Title - Clinical Data Associate

Mayo ClinicCompany Name - Mayo Clinic

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Jacksonville, Florida, USA

Full-time

Job Description Under the direct supervision of the study team and research leadership, assists in coordinating the details of the study and documentation concerning study protocols, patient scheduling, retrospective & prospective chart work, data collection, data entry, data management, follow-up information, and compliance with federal, state, sponsor, and institutional guidelines. Overview for the Clinical Data Associate I: The CDA I provides data management support for clinical trials. The

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Lake Success, New York, USA

Full-time

Clinical Research AssociateJob Title - Clinical Research Associate

Zachary Piper Solutions, LLCCompany Name - 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

Clinical Business Systems Analyst - D/T NYC, onsiteJob Title - Clinical Business Systems Analyst - D/T NYC, onsite

Winston Staffing ServiceCompany Name - Winston Staffing Service

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New York, New York, USA

Contract

A clinical business analyst plays a crucial role in healthcare organizations by analyzing clinical data and operations to improve business performance and ensure regulatory compliance. Duties & Responsibilities Analyze and document business requirements and processes; communicate requirements to technical personnel through the construction of basic conceptual data, process models and flowcharts, and technical specifications.Interview end users, stakeholders, and project sponsors in order to ass

Clinical Research AssociateJob Title - Clinical Research Associate

Zachary Piper Solutions, LLCCompany Name - 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

Bidirectional Clinical Data Exchange ArchitectJob Title - Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.Company Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Sr. Clinical SAS ProgrammerJob Title - Sr. Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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 Editing Coding Analyst | Remote | ContractJob Title - Clinical Editing Coding Analyst | Remote | Contract

Walker HealthforceCompany Name - Walker Healthforce

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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, investig