Clinical Research jobs in Remote

Clinical Research Associate (Portuguese Fluency)

Boston, Massachusetts

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Research Associate (Portuguese Fluency) for a Contract assignment with one of our premier Healthcare clients in Boston, MA. * 70% will be traveling to and from sites and 30% will be completed remote at home* Responsibilities : Ability to prioritize workload and manage multiple protocols Contribute to the identification of new sites for clinical trials Implement complete site management including monitoring visits and regu

Contract

USD 65.00 - 80.00 per hour

Clinical Research Scientist III - (Director/Assoc. Director level)

Remote or Hybrid in Parsippany-Troy Hills, New Jersey

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10d ago

Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. Participates in protocol review discussions concerning scientific and procedural aspects of study design. Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision. With supervision, contributes to the design and development of CRFs, Data Management Manuals and Da

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Third Party, Contract

$100 - $110

Field Clinical Research Associate

Tampa, Florida

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3d ago

Associate, Maplegrove, MN Role Summary The Field Clinical Research Associate (Field CRA) is responsible for monitoring clinical research sites to ensure compliance with study protocols, ICH-Google Cloud Platform requirements, applicable regulatory requirements, and sponsor procedures. The Field CRA serves as the primary monitoring resource for assigned sites, conducting routine site visits, reviewing study documentation, identifying risks and compliance concerns, and driving timely resolution

Full-time, Third Party

Depends on Experience

Clinical Research Coordinator

Kalamazoo, Michigan

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Research Coordinator for a Contract to hire assignment with one of our premier Healthcare clients in Kalamazoo, MI. Responsibilities : Prepare, submit, and monitor documentation for research programs. Ensure compliance with research regulations and protocols through audits. Advise caregivers on program design, treatment administration, and patient follow-up. Organize study files, including regulatory binders and source d

Contract

USD 30.00 - 38.00 per hour

Clinical Research Specialist

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking a Clinical Research Specialist for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This position is hybrid. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of ot

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Contract

Clinical Research Professional, Division of Rheumatology, Allergy & Immunology

Cincinnati, Ohio

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Today

Current UC employees must apply internally viaSuccessFactors Next Lives at the University of Cincinnati Founded in 1819, the University of Cincinnati ranks among the nation?s best urban public research universities. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called ?the most ambitious campus design program in the country." UC\'s momentum has n

Full-time

Clinical Research Professional, Division of Rheumatology, Allergy & Immunology

Cincinnati, Ohio

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Today

Full-time

Research Assistant/Customer Service Representative/Clinical Research Coordinators

San Diego, California

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10d ago

We are seeking engaging and detail-oriented Moderators to facilitate research sessions with participants from the general public. This role is responsible for ensuring a positive participant experience while collecting high-quality, unbiased data in accordance with established research protocols. Key Responsibilities Facilitate research studies, interviews, and testing sessions with recruited participants.Guide participants through study activities while ensuring adherence to client protocols an

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Contract

$20 - $30

Director/Senior Director - Program Management - Medical affairs

Remote

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5d ago

Director/Senior Director - Program Management - Medical affairsLocation: Remote / client-facing; NJ preferred Department: Life Sciences Services Employment Type: Full-time About SaamaSaama focuses on the specialized needs of pharmaceutical and biotechnology companies, delivering transformative business outcomes through AI, advanced analytics, deep life-sciences expertise, and collaborative solution development. Our teams work with global life-sciences organizations to solve complex clinical, med

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Full-time, Third Party

Depends on Experience

Sr Mgr, Project Management- AI Clinical Research

Pleasanton, California

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Today

Job Summary: We are seeking an Executive Director to serve as the senior operational and strategic leader for a large, multi-center, multi-year AI initiative focused on one of the largest and most robust evaluations of agentic AI solutions ever conducted. The program is funded by the U.S. Government and involves Kaiser Permanente health system leadership, external vendors, and federal stakeholders with a specific focus on optimization heart failure care at scale within a real world, integrated

Full-time

USD 178,200.00 - 230,560.00 per year

Clinical Safety Monitor

Maple Grove, Minnesota

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3d ago

Monitor, Maplegrove, MN Role Summary The Safety Monitor ensures that clinical studies are planned and conducted in compliance with applicable regulations, Good Clinical Practices, and standard operating procedures. The primary focus of this role is the processing and review of adverse events, ensuring the consistency, completeness, and regulatory compliance of safety data for assigned studies. Key Responsibilities Processes all adverse events per the Clinical Investigational Plan (CIP) and

Full-time, Third Party

Depends on Experience

Principal Clinical Information Analyst

Maple Grove, Minnesota

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3d ago

Analyst,Plano, TX, Maplegrove, MN Role Summary The Principal Clinical Information Analyst is a senior-level individual contributor responsible for leading the design, development, optimization, governance, and strategic evolution of clinical trial reporting and analytics solutions. This role serves as a trusted advisor and subject matter expert for clinical operations, study management, site management, data review, safety, and other shared service functions. The Principal Clinical Information

Full-time, Third Party

Depends on Experience

Lab Technician

San Diego, California

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3d ago

Job: Lab Technician, Neuroscience Biomarkers Immunoassays Duration: 08/31/2026 to 12/31/2026 with possible extension Location: San Diego, CA 92121 (Onsite) Description: The Lab Technician, Biomarkers Protein Lab is a member of the Neuroscience Precision Biomarkers team, and is responsible for creating and validating assays, executing them, planning experiments, and implementing immunoassays on clinical samples. They maintain equipment and ensure laboratory safety by identifying problems and co

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Contract

$33 - $38

Lab Technician, Neuroscience Biomarkers Immunoassays

San Diego, California

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3d ago

We are looking for Lab Technician, Neuroscience Biomarkers Immunoassays for our client in San Diego CA. Job Title: Lab Technician, Neuroscience Biomarkers Immunoassays Job Location: San Diego CA Job Type: Contract Job Overview: Pay Range: $33.73hr - $38.73hr Requirement/Must Have: Bachelor s degree (B.S) in Science, Engineering, or Technical subjects.3+ years of experience in a Biological/Chemistry discipline.Prior experience with sample handling.Experience with NuLisa, ELISA, and/or Simoa.Exper

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Contract, Third Party

Depends on Experience

Clinical Study Assistant

Remote or New Brunswick, New Jersey

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Today

Clinical Study Assistant Kelly Science and Clinical FSP is currently seeking a Clinical Study Assistant (CSA) for a long-term engagement with one of our Global Medical Device clients. This position is remote in eastern time zone. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Denta

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Contract

Coverage Analyst III

Sacramento, California

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Coverage Analyst for a Contract assignment with one of our premier Healthcare clients working remotely. Responsibilities : The Coverage Analyst will provide temporary remote support to Institute's Clinical Trials Administration team during Epic Research Modernization and Stanford-Sutter JVCC readiness. The role will focus on clinical research coverage analysis, protocol review, billing calendar development, study startup, workflo

Contract

USD 40.00 - 60.00 per hour

SME - Reviewer Scientist

Remote

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5d ago

Subject Matter Expert - Reviewer ScientistThe SME - Reviewer Scientist will provide scientific and regulatory expertise in reviewing clinical and nonclinical data submitted in support of drug applications. This position will support projects within the FDA Center for Drug Evaluation and Research (CDER), Office of Computational Science, under the direction of the COR. Responsibilities: Review clinical safety and efficacy studies submitted in support of drug applications. Evaluate clinical and non

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Full-time

Depends on Experience

Clinical Study Administrator

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be e

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Contract

Contract role: Senior Clinical SAS Developer at North Wales, PA (Onsite) - C2C

Hybrid in North Wales, Pennsylvania

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Today

Senior Clinical SAS Developer Upper Gwynedd, PA (Onsite) C2C is fine Looking for SDTM experts having in-depth knowledge of SAS programming(macro's) Must have 10+ yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point of contact for biostatisticians and study teams Perform peer review of code and documentation for accuracy and traceability Review CRF (Case Report Form) annotatio

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Third Party, Contract

Data Scientist II

Dallas, Texas

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Today

WHY UT SOUTHWESTERN? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goa

Full-time