clinical trial management system Jobs

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Application Analyst - EPIC Research

Memorial Sloan Kettering Cancer Center

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New York, New York, USA

Full-time

Pay Range: $111,600.00-$178,600.00 Company Overview: The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a diseas
Posted 9 days ago | Updated 2 hours ago

Clinical Research Coordinator

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
Posted 3 days ago | Updated 11 hours 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 6 days ago | Updated 11 hours ago

Clinical QA Lead

Bahwan CyberTek Inc.

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Boston, Massachusetts, USA

Contract, Third Party

Title : Clinical QA Lead Location: Boston, MA (Hybrid) Duration : Long term Description: Minimum of 8 years of software quality testing experience and 12+ years IT/Industry experience. 5+ years of experience in Computer Systems Validation (CSV) in the context of Good Clinical/Manufacturing Practices (GxP) is preferred. Experience with software application test planning and functional testing, performance testing, developer management, and defect management using Application lifecycle management
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Posted 1 day ago

Sr. Analyst, US Transparency Reporting

INSPYR Solutions

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King of Prussia, Pennsylvania, USA

Contract

Title: Sr. Analyst, US Transparency Reporting Location: King of Prussia, PA - Hybrid onsite Duration: 3 Months + Compensation: $49.00 - $70hr Work Requirements: , Holders or Authorized to Work in the U.S.Sr. Analyst, US Transparency Reporting - (Data Analyst with Healthcare Financial and Spendata exp.)Shift/Schedule Details: Standard Business Hours - Hybrid Schedule Specifics: Role is located in King of Prussia, PA; hybrid with up to 60% remote; 2 days per week required onsite (Tuesday strongly
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Posted 20 hours ago | Updated 8 hours ago

SCI CTO Trial Activation Specialist (Hybrid)

Stanford University

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Remote or Stanford, California, USA

Full-time

Stanford Cancer Institute - Clinical Trials Office Research Services Trial Activation Lead - Hybrid Position The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over
Posted 13 days ago | Updated moments 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 33 days ago | Updated moments ago

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Responsible for data management documentation, including, but not limited to data management plan(DMP), CRF, eCRF design, edit check specifications, data issue logs, and data review plans and ensures all documents follow study design and regulatory requirements. Maintain Data Management outsourcing metrics and key performance indicators to aid the selection of CRO partners / Vendors and the ongoing management of partnerships. Participate in vendor qualifications and audits.
Posted 29 days ago | Updated moments ago

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

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Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana
Posted 29 days ago | Updated moments ago

IT Product Manager - Clinical Systems

Eli Lilly and Company

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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 31 days ago | Updated moments ago

Senior Consultant, Management Information Services - Level B, Clinical Operations

NYC Health & Hospitals Corporation

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New York, New York, USA

Full-time

Empower Every New Yorker - Without Exception - to Live the Healthiest Life Possible NYC Health + Hospitals is the largest public health care system in the United States. We provide essential outpatient, inpatient and home-based services to more than one million New Yorkers every year across the city's five boroughs. Our large health system consists of ambulatory centers, acute care centers, post-acute care/long-term care, rehabilitation programs, Home Care, and Correctional Health Services. Our
Posted 2 days ago | Updated 9 hours ago

Clinical Development Scientist

Daddy Recruiter LLP

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Bothell, Washington, USA

Contract

Job Title - Clinical Development Scientist; This is a hybrid role. 3 days/week in office (bothell or cambridge locations). I am open to candidates in Plymouth (MN) as well. Notes from the manager: I need a PHD or MD candidate who has a scientist background - This is a requirement. I need someone who has worked in the medical device space who has designed studies for regulatory environments. Reporting protocols experience within this industry also required. US Regulations experience is required
Easy Apply
Posted 2 days ago

Clinical Systems Specialist

Tandym Tech

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Woburn, Massachusetts, USA

Contract

A biotech company in Massachusetts has a great Remote contract opportunity awaiting a new Clinical Systems Specialist. In this role, the Clinical Systems Specialist will be responsible for supporting the lifecycle management of clinical systems for Global Development Operations. To be considered for this opportunity, the qualified professional must be able to work on a W2 basis. Responsibilities: Work on planning, design, configuration, and deployment of new clinical systems and enhancements
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Posted 23 days ago | Updated 1 hour ago

Clinical Informatics Support Analyst

Futrend Technology

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Bethesda, Maryland, USA

Full-time

Futrend Technology has an opening for a Clinical Informatics Support Analyst to join our team of professionals in support of one of our customers in a Clinical Health Care environment. About Futrend: Futrend Technology, Inc. is a business and technology solutions provider. Our primary focus and core competencies are in Healthcare IT and program support. We excel at providing customers with high-value solutions that support their missions and meet their most critical objectives and business need
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Posted 10 days 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 15 days ago | Updated 19 hours ago

Clinical Development Scientist

ComTec Information Systems

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Bothell, Washington, USA

Contract

Clinical Development Scientist Hybrid role. 3 days/week in office Bothell WA/Cambridge MA/ Plymouth MN 12 Months Ultrasound, Senior Clinical Development Scientist The Senior Clinical Development Scientist for the Ultrasound group will be responsible for developing, generating, and disseminating clinical and economic evidence ensuring innovation, and transformation with best-in-class clinical evidence. Your role: Contribute strategic guidance for clinical and economic evidence related to the en
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Posted 10 days ago

Epic Ancillary Clinical Application Analyst

Apidel Technologies

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Newport Beach, California, USA

Contract

Job Title: Ancillary Clinical Application Analyst Working Hours: 7 AM-5 PM Location: Newport Beach, CA 92663 Duration: 06- Contract Months [Potential for Extension based on performance and project needs] Top Skills: Certifications in EPIC and third-party apps are not important; the manager wants to see candidates with knowledge of integrations with EPIC and third-party apps.We will be focused on backend implementation and testing, and we must be strong.Job Description: The Applications Analyst
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Posted 24 days ago | Updated 6 days 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 10 hours 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 10 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 27 days ago | Updated moments ago