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ARC Health Partners
Overview
The TMS Technician assists in the delivery of Transcranial Magnetic Stimulation therapy by preparing patients, monitoring treatment sessions, and ensuring patient comfort. They are responsible for maintaining accurate medical documentation, adhering to safety and infection control standards, and communicating patient progress to the supervising provider.
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Compensation
$23 - $25 / HOUR
Posted
3 days ago
The TMS Technician assists in the delivery of Transcranial Magnetic Stimulation therapy by preparing patients, monitoring treatment sessions, and maintaining accurate medical documentation. They ensure a safe, therapeutic environment while troubleshooting equipment and communicating patient progress to the supervising medical provider.
$22 - $24 / HOUR
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
9 days ago
M3USA
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the Investigator with participant screening, maintaining documentation, collecting and entering data, and overseeing other research staff.
$30 - $40 / HOUR
16 days ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
Salary not listed
Imperative Care
Provide in-house clinical operations support by managing study documentation, site coordination, and day-to-day trial activities. Conduct clinical monitoring and data verification to ensure high-quality execution and regulatory compliance across trial sites.
$101,000 - $106,000 / YEAR
23 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.
25 days ago
StageBio
Perform essential histology duties including tissue grossing, processing, embedding, microtomy, and staining. Maintain a safe working environment and ensure accurate data recording in compliance with SOPs.
$19 - $28 / HOUR
Syneos Health
Provide patient-focused clinical services including mobile research nursing and patient concierge for pharmaceutical and biotechnology industries. Support clinical trials across various phases and therapeutic areas to improve the patient experience.
$67,700 - $115,100 / YEAR
1 month ago
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with participant screening, maintaining documentation, and ensuring all activities comply with the research protocol and regulations.
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening study participants, maintaining documentation, and ensuring compliance with research protocols.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with screening, maintaining documentation, collecting and entering data, and mentoring junior staff.
GRAIL
The Clinical Project Assistant supports study teams in Clinical Operations by managing administrative aspects of clinical trial execution. Key duties include maintaining the Trial Master File, tracking site payments, and assisting with quality metrics and meeting coordination.
$33 - $39 / HOUR
Fortrea
The CRA will lead and support the Medical Device & Diagnostics team by managing all aspects of study site monitoring, including routine visits and close-outs. They are responsible for ensuring protocol adherence, data integrity, and the protection of study participants through rigorous clinical research standards.
$105,000 - $117,000 / YEAR
Johnson & Johnson Innovative Medicine
The Clinical Trials Assistant supports the clinical study team with project communications, site payments, and file management. They are responsible for maintaining clinical databases, processing regulatory documents, and ensuring study supplies are managed effectively.
$41,000 - $66,700 / YEAR
ROM TECHNOLOGIES INC
The individual will develop and implement clinical protocols for pilot programs and IRB studies while delivering therapy to patients. They will also collaborate with research teams and represent the company to healthcare leaders to demonstrate clinical value.
$85,000 - $100,000 / YEAR
The CRA 2 is responsible for all aspects of study site monitoring, including routine visits, site management, and maintenance of study files. They ensure protocol adherence, data integrity, and the protection of study participants while managing serious adverse event reporting.
