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Evolution Research Group
Overview
The Assistant Clinical Research Coordinator supports the collection, documentation, and analysis of clinical research data for Phase I-IV trials. They perform clinical tasks including venipuncture and ECGs while ensuring study protocols and patient safety guidelines are followed.
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Compensation
Salary not listed
Posted
2 days ago
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.
9 days ago
The Patient Care Technician oversees the care of clinical trial subjects and performs medical procedures including blood collection and ECGs. They are responsible for sample processing, documentation, and maintaining a safe environment in accordance with regulatory guidelines.
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 Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample processing. They are responsible for dispensing investigational products and maintaining accurate documentation in subject charts according to protocol.
$39 - $45 / HOUR
The Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample collection. They are responsible for documenting subject data and ensuring compliance with Good Clinical Practices and doctor's orders.
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.
The Research Assistant will support clinical teams by performing patient assessments, including vitals and phlebotomy, and managing study documentation. They are also responsible for data entry, specimen processing, and maintaining lab kit inventory in compliance with FDA and GCP regulations.
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.
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 Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They ensure protocol adherence, manage subject recruitment, and maintain accurate regulatory documentation under the direction of the Principal Investigator.
Headlands Research
The CRC manages and executes Phase I-IV clinical studies from site initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
The Clinical Research Coordinator manages and executes Phase I-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaboration with investigators and sponsors.
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
Medpace, Inc.
The Clinical Nurse will provide necessary nursing coverage for the Clinical Pharmacology Unit, adhering strictly to study protocols and Good Clinical Practice guidelines. Responsibilities include performing and documenting various clinical procedures, safely administering medications, assessing adverse events, and providing detailed end-of-shift reports for continuity of care.
24 days ago
Roche
Act as a field medical partner providing scientific information on CVRM pipeline medicines to healthcare providers and experts. Manage clinical trial activities including site selection, recruitment, and retention while gathering customer insights for internal stakeholders.
$161,000 - $299,000 / YEAR
25 days ago
CenExel
Provide therapeutic support and psychedelic-assisted therapy for participants in clinical research trials. Ensure patient safety during sessions and support the integration of experiences according to study protocols.
$200 / HOUR
27 days ago
