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Solaris Health Holdings LLC
Overview
The Clinical Research Assistant provides hands-on clinical support by collecting patient vitals and biological samples while managing study documentation and data entry. They also streamline operations by scheduling scans, managing supplies, and ensuring adherence to research protocols.
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Compensation
Salary not listed
Posted
3 days ago
Alcanza Clinical Research
Acts as a Sub-Investigator to perform physical and medical history assessments and manage subjects in clinical research trials. Coordinates daily research activities according to SOPs, GCP, and FDA/ICH guidelines while ensuring patient safety and welfare.
10 days ago
Platinum Dermatology Partners LLC
Responsible for the administrative and clinical execution of research studies, including subject recruitment, screening, and data collection. The role involves coordinating with physicians to perform procedures and ensuring strict adherence to FDA, GCP, and IRB guidelines.
$27 - $30 / HOUR
11 days ago
COMPREHENSIVE EYECARE PARTNERS LLC GROUP
The Clinical Research Technician coordinates and executes clinical research studies while ensuring strict adherence to protocols and regulatory guidelines. Key duties include managing patient eligibility, documenting adverse events, and entering study data into Case Report Forms.
16 days ago
COMPREHENSIVE EYECARE PARTNERS LLC
The Clinical Research Technician coordinates and executes clinical research studies while ensuring strict adherence to protocols and regulatory guidelines. Responsibilities include managing patient eligibility, documenting adverse events, and entering study data into Case Report Forms.
University of Chicago
Manages moderately complex clinical trials, including subject recruitment, screening, and data collection. Ensures strict adherence to protocols, regulatory compliance, and maintains communication between sponsors and the Principal Investigator.
$60,000 - $75,000 / YEAR
The Clinical Research Nurse ensures the execution of assigned studies by performing clinical procedures and managing patient follow-up visits. Responsibilities include documenting in source charts, entering data into EDC, and maintaining compliance with FDA and GCP regulations.
25 days ago
The Clinical Research Nurse ensures the execution of assigned studies by performing clinical procedures and patient follow-ups. Responsibilities include screening patients, documenting in source charts, and maintaining compliance with FDA and GCP regulations.
Responsible for the administrative and clinical execution of research studies, including subject recruitment, screening, and data management. Provides direct support to Principal Investigators by assisting with medical procedures and ensuring compliance with FDA and IRB guidelines.
$28 - $31 / HOUR
1 month ago
The Clinical Research Coordinator is responsible for managing administrative aspects of clinical trials, including subject recruitment, screening, and enrollment. They also assist physicians with clinical procedures and ensure all study activities comply with FDA, GCP, and IRB guidelines.
$30 - $33 / HOUR
Woman's Hospital
The Research Coordinator manages clinical trial procedures, including data collection, regulatory documentation, and participant consent. They collaborate with medical staff to ensure accurate study implementation and maintain high-quality data standards.
$21 - $33 / HOUR
IQVIA
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
The Senior CRA is responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. They conduct site visits, support subject recruitment, and maintain essential study documentation to ensure data integrity.
$87,200 - $169,300 / YEAR
The Clinical Research Coordinator is responsible for managing administrative aspects of clinical trials, including subject recruitment, screening, and enrollment. They also assist physicians with clinical procedures, maintain study documentation, and ensure compliance with FDA, GCP, and IRB guidelines.
2 months ago
The coordinator will manage all aspects of clinical trials, including screening, enrollment, subject follow-up, and maintaining accurate documentation for compliance and study administration. Responsibilities also involve performing protocol procedures, educating patients, monitoring adverse events, and organizing site visits.
$50,000 - $65,000 / YEAR
Structure Therapeutics
The Sr. CRA will independently manage clinical aspects of studies, ensuring adherence to GCPs, SOPs, and protocols while working closely with cross-functional teams, vendors, and sites. Key duties include overseeing study execution from start-up to closeout, managing vendor deliverables, and acting as a point of escalation for site monitoring activities.
$135,000 - $150,000 / YEAR
4 months ago
The Sr. CRA will independently manage clinical aspects of studies, ensuring adherence to GCPs, SOPs, and protocols while working closely with cross-functional teams, vendors, and sites. Key duties include overseeing study execution from start-up to closeout, managing vendor activities, and acting as a point of escalation for clinical sites.
