Entry Level Clinical Analyst Jobs

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Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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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 3 days ago | Updated 2 hours ago

Clinical Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem)

CEDARS-SINAI

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Los Angeles, California, USA

Full-time

Job Description When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite you to consider this phenomenal opportunity! Dr. Pramod Butte, Ph.D. is looking for a Clinical Research Associate I to join a diverse team! The primary focus of the Butte Laboratory is translational research in the field of bio-photonics. The But
Posted 2 hours ago | Updated 1 hour ago

Clinical Trial Manager

Advanced Recruiting Partners

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Raleigh, North Carolina, USA

Full-time

Job DescriptionKey Responsibilities: Lead and manage all operational aspects of global clinical trials from study start-up through close-outOversee study timelines, deliverables, and budgets to ensure milestones are metCoordinate with cross-functional teams, external vendors, and CROs to ensure high-quality study conductOversee site activation, clinical monitoring, data integrity, and adherence to protocolConduct study-level risk assessments and ensure inspection readinessManage safety and pharm
Posted 9 days ago | Updated 1 hour ago

Clinical Research Data Specialist I - Per diem - Heart Institute

CEDARS-SINAI

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Los Angeles, California, USA

Full-time

Job Description When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai, and it's just one of the many reasons why we rank as one of the top hospitals in the nation by U.S. News & World Report. From working with a team of committed healthcare professionals to using innovative facilities, you'll have everything vital do something
Posted 2 hours ago | Updated 1 hour 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 30 days ago | Updated 20 days ago

Manager-Vendor Performance Management(Clinical)

NexInfo Solutions, Inc.

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Morris Plains, New Jersey, USA

Contract, Third Party

About Nexinfo: NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges
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Posted 19 days ago | Updated 18 days ago

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
Posted 10 days ago | Updated 2 hours ago

Clinical Data Manager

Tandym Tech

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Woburn, Massachusetts, USA

Contract

A pharmaceutical company in Massachusetts is currently seeking a new Clinical Data Manager to provide Data Management support for assigned programs. Responsibilities: Work with Clinical Data Management (CDM) Lead to support operational activities for one or more programs Monitor data management vendor quality of work through key performance metrics Maintain program level DM deliverable timelines in accordance with program development strategy Support data management at cross-functional team mee
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Posted 21 days ago | Updated 7 hours ago

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
Posted 14 days ago | Updated 2 hours ago

Clinical Project Manager SME with AI/ Gen experience-Hybrid@NY

BURGEON IT SERVICES LLC

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New York, New York, USA

Third Party, Contract

Role: Clinical Project Manager SME with AI/ Gen experience Location: New York city, NY Hybrid. Long term contract Domain: Life Science Clinical R&D + Gen AI + 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 geograph
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Posted 4 days ago

Remote Clinical Ancillary Solution Consultant/Lead

Infinite Computer Solutions (ICS)

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Remote

Full-time

Note : GCEAD, L2EAD, consultant can apply for this position who can work on W2. Job Descriptions : Core Responsibilities: Architect solutions for inpatient (eMAR, PowerForms, PowerPlans) and specialty streams (OB module, ED triage, Perioperative).Support Materials Management, CBORD nutrition, and Clairvia staffing interfaces (FHIR, HL7) across all ancillary services.Oversee custom Discern CCL and DA2 rule development for clinical decision support, alerts, and advanced reporting.Collaborate wi
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Posted 34 days ago | Updated 13 days ago

Clinical Research Coordinator

Eximia Research

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Murfreesboro, Tennessee, USA

Full-time

Job DescriptionCompany Description Eximia Research is a fully Integrated research sites network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). Our premier, multidisciplinary wholly owned research sites located across country and known for excellent trial execution, rapid subject recruitment/enrollment and delivery of a quality data. Clinical Research Coordi
Posted 8 days ago | Updated moments ago

Clinical Research Coordinator (Neuro-Psychiatric)

Eximia Research

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Raleigh, North Carolina, USA

Full-time

Job DescriptionCompany Description Eximia Research is a fully Integrated research sites network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). Our premier, multidisciplinary wholly owned research sites located across country and known for excellent trial execution, rapid subject recruitment/enrollment and delivery of a quality data. Clinical Research Coordi
Posted 8 days ago | Updated moments ago

Veeva Clinical Data Tester - Remote

Smart Source Technologies

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Remote

Contract

Veeva Clinical Data Management Tester Location : Fully Remote Duration : 12 months contract + extension Pay rate : $50/hr W2 (All Incl) Key requirements: Proficiency in CDMSExpertise in EDCHands-on experience in full cycle testing with Veeva
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Posted 10 days ago | Updated 5 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 39 days ago | Updated 4 days ago

Field Clinical Engineer

FemPulse Corporation

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Sunnyvale, California, USA

Full-time

Job DescriptionFemPulse is a Bay Area-based med-tech startup seeking an experienced, skilled, and compassionate Field Clinical Engineer (FCE) to support an FDA IDE pivotal clinical trial of a novel, non-implanted neuromodulation device for overactive bladder (OAB) in women. The FCE will be responsible for timely execution of our clinical trial including interacting with study participants during study visits, partnering with study staff to ensure compliance to FDA regulations and troubleshooting
Posted 19 days ago | Updated 1 day ago

Field Clinical Engineer

FemPulse Corporation

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Santa Rosa, California, USA

Full-time

Job DescriptionFemPulse is a Bay Area-based med-tech startup seeking an experienced, skilled, and compassionate Field Clinical Engineer (FCE) to support an FDA IDE pivotal clinical trial of a novel, non-implanted neuromodulation device for overactive bladder (OAB) in women. The FCE will be responsible for timely execution of our clinical trial including interacting with study participants during study visits, partnering with study staff to ensure compliance to FDA regulations and troubleshooting
Posted 19 days ago | Updated 12 hours ago

Field Clinical Engineer

FemPulse Corporation

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Santa Clara, California, USA

Full-time

Job DescriptionFemPulse is a Bay Area-based med-tech startup seeking an experienced, skilled, and compassionate Field Clinical Engineer (FCE) to support an FDA IDE pivotal clinical trial of a novel, non-implanted neuromodulation device for overactive bladder (OAB) in women. The FCE will be responsible for timely execution of our clinical trial including interacting with study participants during study visits, partnering with study staff to ensure compliance to FDA regulations and troubleshooting
Posted 19 days ago | Updated 12 hours ago

Field Clinical Engineer

FemPulse Corporation

•

San Mateo, California, USA

Full-time

Job DescriptionFemPulse is a Bay Area-based med-tech startup seeking an experienced, skilled, and compassionate Field Clinical Engineer (FCE) to support an FDA IDE pivotal clinical trial of a novel, non-implanted neuromodulation device for overactive bladder (OAB) in women. The FCE will be responsible for timely execution of our clinical trial including interacting with study participants during study visits, partnering with study staff to ensure compliance to FDA regulations and troubleshooting
Posted 19 days ago | Updated moments ago

Field Clinical Engineer

FemPulse Corporation

•

Sonoma, California, USA

Full-time

Job DescriptionFemPulse is a Bay Area-based med-tech startup seeking an experienced, skilled, and compassionate Field Clinical Engineer (FCE) to support an FDA IDE pivotal clinical trial of a novel, non-implanted neuromodulation device for overactive bladder (OAB) in women. The FCE will be responsible for timely execution of our clinical trial including interacting with study participants during study visits, partnering with study staff to ensure compliance to FDA regulations and troubleshooting
Posted 19 days ago | Updated moments ago