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Arizona Liver HealthNew
Overview
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
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Compensation
$28 - $36 / HOUR
Posted
New
Iterative Health
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
Salary not listed
2 days ago
Mid-Atlantic Permanente Medical Group PC
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required assessments. They also ensure regulatory compliance by preparing IRB submissions and maintaining accurate study documentation throughout the lifecycle.
$79,370 - $99,213 / YEAR
4 days ago
Nevada System of Higher Education
The Research Coordinator will recruit and screen clinical trial participants, manage regulatory documentation, and provide clinical care services including patient monitoring and sample processing. They will also assist with study budget proposals, data entry, and ensure adherence to institutional and federal protocols.
$25 - $37 / HOUR
8 days ago
Stormont Vail Health
Perform blood specimen collection via venipuncture and capillary puncture for patients across various acute care settings. Manage test orders through electronic medical records and perform waived point of care testing.
14 days ago
The Clinical Research Coordinator manages industry-sponsored clinical trials, including patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and investigators.
The Clinical Research Coordinator manages the daily activities of industry-sponsored clinical trials, including patient recruitment and visit coordination. They are responsible for clinical tasks like blood draws and ECGs, while ensuring strict adherence to study protocols and regulatory guidelines.
The CRC II manages industry-sponsored clinical trials, overseeing patient recruitment, study visits, and the collection of clinical data. They are responsible for maintaining high-quality documentation and coordinating communication between sponsors, CROs, and the Principal Investigator.
The CRC II manages industry-sponsored clinical trials by coordinating daily activities, leading patient recruitment, and conducting study visits. They are responsible for specimen processing, data entry into CTMS, and maintaining communication with sponsors and PIs.
The Clinical Research Coordinator manages industry-sponsored clinical trials, focusing on patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and investigators.
The Clinical Research Coordinator II manages daily clinical trial activities, including protocol management, patient recruitment, and study visit coordination. They are responsible for ensuring data integrity, maintaining regulatory documentation, and serving as the primary point of contact for study participants.
The Senior Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures. They also ensure accurate data entry, maintain study documentation, and coordinate with sponsors and investigators to meet enrollment targets.
MyMichigan Health
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and act as a liaison between investigators, sponsors, and participants.
22 days ago
The CRC II manages industry-sponsored clinical trials, focusing on patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and PIs.
Caring Hands United, Inc.
As a caregiver, you will provide essential services to help elderly individuals and those with disabilities live independently in their homes. Responsibilities include personal care, assistance with daily activities, medication reminders, and emotional support.
25 days ago
City of Hope
The Clinical Research Nurse coordinates oncology clinical trials, managing everything from patient recruitment and informed consent to data collection and biospecimen handling. They ensure strict adherence to federal regulations, study protocols, and institutional SOPs to protect human subjects.
28 days ago
Best Care
Coordinates clinical research studies including regulatory compliance, study start-up, subject follow-up, and record maintenance. Manages trial oversight, participant safety, and the handling of investigational products.
IRONWOOD PHYSICIANS,P.C.
Manages and coordinates all clinical and administrative aspects of conducting clinical trials in accordance with protocol guidelines and federal regulations. Acts as a liaison between investigators, sponsors, and the IRB while performing patient procedures and assessments.
Tufts Medicine
Assist the Principal Investigator in planning and implementing clinical research studies, including participant recruitment and screening. Manage study documentation, regulatory compliance, and data entry while ensuring adherence to IRB and FDA guidelines.
$47,924 - $59,895 / YEAR
29 days ago
The Clinical Research Coordinator assists in planning and implementing cardiovascular clinical research studies, including participant recruitment, screening, and data collection. They are responsible for maintaining regulatory compliance, managing study documentation, and ensuring patient safety throughout the research process.
