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Clinilabs
Overview
The Polysomnographic Technologist prepares and collects data for research and clinical duties, ensuring the accuracy of recording procedures. Responsibilities also include direct contact with subjects for assessments and maintaining laboratory equipment.
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Compensation
$47 - $55 / HOUR
Posted
6 days ago
Evolution Research Group
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.
Salary not listed
9 days ago
The EMT/Paramedic assists in clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing ECGs, venipuncture, and ensuring all procedures follow Good Clinical Practices (GCP).
The LPN assists in clinical trials by dispensing investigational drugs and collecting biological samples. Responsibilities include performing venipuncture, ECGs, and ensuring compliance with Good Clinical Practices (GCP).
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 LPN or RN will assist in the conduct of clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing clinical procedures, maintaining accurate subject charts, and ensuring compliance with Good Clinical Practices.
The Patient Care Technician oversees the care of clinical trial subjects and performs medical procedures including blood collection and ECGs. They are responsible for maintaining a safe environment and ensuring compliance with GCP and ICH guidelines.
The Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample collection. They are responsible for dispensing medications, documenting subject data, and maintaining a safe, compliant work environment according to study protocols.
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.
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.
13 days ago
ICON plc
The Clinical Research Nurse I will support the execution of clinical trials by assisting in planning, implementation, and coordination of research activities while conducting patient assessments and administering study treatments. This role involves collecting, recording, and maintaining accurate patient data in eCRFs and collaborating with multidisciplinary teams to ensure efficient study conduct and participant retention.
17 days ago
Care Access
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
21 days ago
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
22 days ago
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 specimens, and maintaining accurate study documentation under the direction of a Coordinator.
23 days ago
The Clinical Research Assistant supports the research process by recruiting participants, conducting screenings, and obtaining informed consent. They are also responsible for collecting and processing specimens, recording data, and maintaining site logs according to protocol.
The Clinical Research Assistant will support the clinical research process by assisting with participant recruitment, screening, and scheduling. They will also perform clinical procedures such as specimen collection and data entry while maintaining adherence to FDA regulations and site protocols.
Oregon Health & Science University
The Senior Clinical Research Assistant manages patients on clinical trials, including consenting, enrolling, and gathering data. They are also responsible for regulatory tasks, sample processing, and assisting the Clinical Research Manager with various projects.
$48,734 - $77,522 / YEAR
24 days ago
Neurocrine Biosciences
Supports Clinical Operations by managing the quality, compliance, and inspection-readiness of Trial Master Files (TMF). Acts as a subject matter expert for eTMF systems, facilitating audits and collaborating with cross-functional teams to maintain study documentation.
$89,800 - $123,000 / YEAR
The coordinator is responsible for screening, enrolling, and monitoring clinical research subjects while ensuring strict adherence to protocols and regulatory guidelines. Key duties include performing clinical procedures, managing study documentation, and coordinating with sponsors and investigators.
