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Mass General Brigham
Overview
Performs donor registration, screenings, whole blood collection, and automated platelet collections. Responsible for maintaining quality control, documenting corrective actions, and transporting blood products to the blood bank.
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Compensation
$23 - $33 / HOUR
Posted
2 days ago
OneOncology
As the Research Nurse, you will screen, enroll, and follow study subjects, ensuring protocol compliance and monitoring. You will also be responsible for source documentation, recording adverse events, and dispensing investigational products.
Salary not listed
3 days ago
Avera Health
Coordinates and implements research study protocols, including participant recruitment, data collection, and laboratory specimen processing. Collaborates with investigators and healthcare providers to ensure safe, compliant research procedures for maternal and child health studies.
$21 - $37 / HOUR
4 days ago
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
$22 - $37 / HOUR
Evolution Research Group
The Psychometric Rater is responsible for administering and scoring clinical tests and managing data collection for clinical trials. They collaborate with researchers to ensure strict adherence to study protocols, ethical guidelines, and FDA regulations.
$30 / HOUR
9 days ago
The Psychometric Rater is responsible for administering and scoring tests for clinical trial participants while ensuring strict adherence to study protocols and ethical guidelines. They collaborate with researchers to collect accurate data and manage participant documentation under the direction of the Principal Investigator.
$34 / HOUR
The Clinical Research Coordinator manages the implementation of clinical trials, including subject screening, enrollment, and the administration of study procedures. They ensure all activities comply with FDA regulations, GCP guidelines, and company SOPs while maintaining accurate study documentation.
The Clinical Research Coordinator manages the implementation of clinical trials, ensuring adherence to protocols and regulatory requirements. They are responsible for screening and enrolling subjects, maintaining accurate study records, and reporting adverse events under the direction of the Principal Investigator.
The Research Assistant is responsible for assisting with clinical research studies, collecting and analyzing data, and ensuring strict adherence to study protocols and FDA regulations. They will also perform clinical tasks such as phlebotomy and ECGs while maintaining accurate study records and managing lab inventory.
Headlands Research
Coordinate all aspects of assigned clinical trials from site initiation to study close-out, ensuring compliance with study protocols and regulations. Manage subject recruitment, conduct visits, and maintain accurate documentation throughout the trial process.
UT Health San Antonio
Manage medication therapy to facilitate patient care within a clinic and infusion room setting. Provide medication-related services to optimize pharmacotherapeutic outcomes and offer remote services to clinic infusion areas.
11 days ago
American Addiction Centers
Provides administrative and operational support to the Alzheimer's Disease Research Center, splitting time between administrative and clinical cores. Key tasks include managing patient appointments, maintaining research logs, and supporting regulatory and financial processes.
$22 - $33 / HOUR
Care Access
Perform clinical tasks including venipuncture and biospecimen processing to support clinical trials. Handle administrative duties such as participant scheduling, data entry, and maintaining site logs.
$24 - $38 / HOUR
13 days ago
The Clinical Research Coordinator II manages the implementation and coordination of clinical trials, ensuring compliance with protocols and regulatory standards. They are responsible for subject recruitment, screening, informed consent, and maintaining accurate study documentation.
St. Elizabeth Healthcare
Coordinate clinical research studies by managing subject enrollment, data collection, and regulatory compliance. Collaborate with physicians to open new studies and ensure adherence to protocol and FDA guidelines.
16 days ago
Nova Medical Services
The Clinical Research Coordinator manages the planning and execution of clinical trials, ensuring strict adherence to ICH, GCP, and regulatory guidelines. Key duties include coordinating patient visits, maintaining regulatory documentation, and managing study data entry and verification.
$23 - $25 / HOUR
17 days ago
SerenaGroup Inc
The Clinical Research Coordinator manages day-to-day clinical trial activities, including patient recruitment, screening, and study visit execution. They are responsible for maintaining accurate study documentation and ensuring compliance with FDA and ICH-GCP guidelines.
20 days ago
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
The Clinical Research Coordinator I, RN conducts delegated clinical tasks and monitors research participants to ensure compliance with protocols and regulations. They are responsible for patient coordination, documentation, and recruitment activities.
The Clinical Research Assistant supports the research process by recruiting participants, conducting screenings, and obtaining informed consent. They are responsible for performing visit procedures, collecting and shipping specimens, and maintaining accurate study documentation.
$19 - $33 / HOUR
21 days ago
