Clinical research coordinator jobs

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 Coordinator

San Antonio, Texas

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Today

Responsibilities: SUMMARY The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The CRC will work collaboratively with the principal investigator (PI), the Sr. Clinical Research Coordinator (SCRC), the clinical site, spons

Full-time

Field Clinical Research Associate

Tampa, Florida

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Today

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 Scientist III - (Director/Assoc. Director level)

Remote or Hybrid in Parsippany-Troy Hills, New Jersey

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5d 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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Contract, Third Party

$100 - $110

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

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

Radiography Clinical Coordinator

San Francisco, California

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Radiography Clinical Coordinator for a Contract assignment with one of our premier Healthcare clients in San Francisco, CA. Responsibilities : Clinical practice knowledge and applied background in a radiology modality Manages site recruitment, student assignment, competency evaluation, preceptor development Knowledge of medical center, HR and UC policies Enforces supervision policy - students directly supervised by an ARRT-certif

Contract

USD 65.00 - 80.00 per hour

Research Assistant/Customer Service Representative/Clinical Research Coordinators

San Diego, California

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6d 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

Research Coordinator

Waltham, Massachusetts

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Today

Description Our client is a company that partners with industry leading teams to conduct studies aimed at advancing scientific knowledge and research and development. They have recruited participants for an in-person study on human communication, focusing on aspects of speech and hearing, such as articulation and timing and are now looking for study moderators to help administer the study. Additional Skills & Qualifications Study moderators serve as the primary on-site point person for managing

Full-time

USD 20.00 - 22.00 per hour

Healthcare Data Analyst, Health and Clinical Outcomes Research (Onsite)

Galveston, Texas

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Today

JOB SUMMARY Responsible for developing, preparing, interpreting, and monitoring moderate-to-complex health process and outcomes data analyses, projections, data modeling, and reports used by system management in decision-making. Develops, implements, and monitors reporting and analysis solutions from multiple databases to ensure efficient processing, up-to-date tools, improved patient experience, and clinical and operational efficiencies. Serves as an expert resource to provide reporting and an

Full-time

Research Moderator/Data Collection Specialist/Participant Coordinator

Atlanta, Georgia

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2d ago

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Contract, Third Party

Depends on Experience

Data Analyst

Washington, District of Columbia

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Today

Georgetown University comprises two unique campuses in the nation's capital. With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to so

Part-time

USD 26.26 - 48.32 per hour

Clinical Scientific Director

Cambridge, Massachusetts

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Today

By clicking the ?Apply? button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda?s and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Scientific Director in our NS Thera

Full-time

Compensation information provided in the description

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

Participant Readiness Coordinator

Los Angeles, California

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Today

Participant Readiness Coordinator About the Role We are seeking a detail-oriented Participant Readiness Coordinator to support an ongoing user research study. This role is responsible for screening participants, collecting vital signs and baseline health metrics, determining study eligibility, and ensuring compliance with standardized protocols. This position is ideal for candidates with experience in participant screening, health assessments, clinical research, or healthcare environments. Ke

Full-time

USD 28.00 - 28.00 per hour

Clinical Database Programmer-Reference Laboratory

Cincinnati, Ohio

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Today

Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team. This position will work in a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Communicate with inte

Full-time

Clinical Contracts Associate

Remote

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Today

(USA), Plano, TX, Maplegrove, MN Role Summary Working under the direction of a manager or senior contracts associate, the Clinical Contracts Associate provides technical assistance in developing, negotiating, reviewing, and processing clinical study and research contracts and budgets. This role solves problems in straightforward situations using technical experience, judgment, and precedent, and is capable of routine negotiations with limited supervision. Key Responsibilities Develops and

Full-time, Third Party

Depends on Experience

Associate Director, Clinical Trial Disclosure & Transparency

King of Prussia, Pennsylvania

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Today

The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides global strategy, drives process excellence, and oversees the delivery of clinical trial disclosure activities including registration, results disclosure and layperson summaries while providing support for transparency activities

Full-time