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Kaiser PermanenteNew
Overview
Facilitates information distribution by drafting routine reports, presentations, and correspondence. Coordinates departmental workflows, schedules meetings for directors, and assists in the execution of small-scale events.
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Compensation
Salary not listed
Posted
New
Provides high-level administrative support by drafting reports, managing calendars, and coordinating small-scale events for directors and their teams. Maintains departmental workflow through data management, office supply inventory, and handling routine and non-routine requests.
ICON plc
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$91,336 - $114,170 / YEAR
2 days ago
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.
3 days ago
Jackson Health
The Senior Imaging Specialist ensures the accuracy, completeness, and regulatory compliance of clinical documentation and scanned medical records. They conduct quality reviews, identify documentation gaps, and collaborate with stakeholders to maintain high-quality data standards.
St. Jude Children's Research Hospital
Design and execute cell-based therapeutic evaluation workflows and validation pipelines for patient-specific genetic conditions. Develop and characterize patient-derived cellular models and validate quantitative molecular assays to evaluate therapeutic efficacy.
$65,520 - $154,960 / YEAR
7 days ago
Evolution Research Group
The Medical Monitor provides safety and medical oversight for clinical trials, ensuring compliance with protocols, GCP, and regulatory requirements. Responsibilities include reviewing safety data, assessing serious adverse events, and providing medical consultancy to study teams.
9 days ago
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They are responsible for ensuring protocol adherence, managing subject recruitment, and maintaining accurate regulatory documentation under the direction of the Principal Investigator.
Albany Medical Center
The HIM Technician supports health information management processes by retrieving, preparing, scanning, and indexing clinical documentation. They ensure compliance with legal and organizational standards while maintaining patient confidentiality.
$40,495 - $52,643 / YEAR
The Christ Hospital Health Network
The Clinical Research Coordinator supports the Principal Investigator by coordinating daily clinical trial activities and ensuring data integrity. They provide guidance on compliance, financial, and personnel aspects of the study to ensure human subject safety.
10 days ago
Weill Cornell Medical College
The psychometrist will administer and score standardized neuropsychological measures for evaluating memory and cognitive disorders, adhering strictly to high-quality administration and scoring procedures. Responsibilities also include assisting with data collection for clinical trials focused on neurodegenerative conditions and maintaining secure, confidential records.
$32 - $36 / HOUR
Systimmune
The role is responsible for end-to-end safety case processing, including intake, triage, and regulatory submissions. It also involves maintaining the PV database, managing CAPAs, and ensuring global compliance and inspection readiness.
$85,000 - $115,000 / YEAR
11 days ago
Ora
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks and collaborate with project managers and investigators to execute research directives.
14 days ago
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators to execute research directives.
Alivation Health, LLC
The role involves coordinating Behavioral Health Research trials, including patient recruitment, conducting trial visits, and maintaining study documentation. The assistant will also perform clinical safety assessments such as blood draws and vital sign monitoring.
$18 / HOUR
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.
15 days ago
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.
Labcorp
The role involves conducting routine and non-routine sample analysis in compliance with SOPs and regulatory guidelines. Responsibilities include maintaining laboratory records, performing equipment maintenance, and assisting in the validation of immunotoxicology assays.
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$110,520 - $138,150 / YEAR
16 days ago
