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Medical University of South CarolinaNew
Overview
The incumbent will coordinate the recruitment, screening, and enrollment of research participants while collecting psychological and biological data. They are also responsible for maintaining regulatory documentation and providing administrative support for grant proposals and publications.
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Compensation
$37,200 - $59,500 / YEAR
Posted
New
Beacon Clinic
Coordinates daily clinical trial activities, ensuring compliance with FDA and OHRP regulations while managing participant screening and data submission. Performs medical assistant duties including phlebotomy, vital signs documentation, and assisting providers with exams.
Salary not listed
2 days ago
IQVIA
The intern supports the preparation, documentation, and management of investigational products for clinical trials under pharmacist supervision. Key duties include managing drug accountability logs, dispensing medications per protocol, and ensuring regulatory compliance with FDA and IRB standards.
$33,000 - $82,600 / YEAR
Iterative Health
The Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures like blood draws and IV administration. They also ensure data integrity, maintain study documentation, and act as the primary point of contact for study participants.
3 days ago
Headlands Research
Lead and oversee clinical trials, ensuring compliance with protocol requirements and regulatory standards. Provide leadership and mentorship to site staff while fostering a culture of inclusivity and professionalism.
6 days ago
The Laboratory Technician performs specimen collection, processing, documentation, and shipment for clinical trials in compliance with GCP and study protocols, while also assisting with vital signs, ECGs, and maintaining laboratory equipment and cleanliness. Responsibilities also include accurate data recording, resolving data queries, monitoring lab inventory, and supporting study preparation activities.
$22 - $26 / HOUR
Cedars-Sinai
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and data collection. They ensure compliance with federal and local regulations while maintaining accurate source documents and reporting study progress.
$27 - $42 / HOUR
7 days ago
The Medical Laboratory Scientist performs high-complexity clinical laboratory testing in areas such as hematology, chemistry, and immunology to support patient care and research. They are responsible for maintaining laboratory equipment, ensuring regulatory compliance, and documenting quality control activities.
$46,200 - $96,200 / YEAR
8 days ago
Bausch+Lomb Companies Inc.
The Senior Principal Research Optometrist will design and lead clinical studies to support the development and launch of innovative eye care products. This role involves applying clinical and research expertise to study design, data analysis, and collaboration across functions.
$130,000 - $200,000 / YEAR
9 days ago
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
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 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 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 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.
The coordinator is responsible for managing all aspects of research protocols to ensure integrity and quality according to GCP guidelines. Key duties include performing visit procedures, managing study supplies, and providing high-level care to study patients.
$70,000 - $75,000 / YEAR
Research Assistants support the execution of clinical trials by assisting with study visits, preparing materials, and collecting data. They work closely with clinical teams to ensure studies run smoothly and in compliance with established protocols.
UTHealth Houston
Coordinate data collection and operations for the SNAK clinical trial, focusing on participant recruitment, enrollment, and retention. Manage study data, administer surveys, and connect families to community-based resources under the supervision of the Primary Investigator.
11 days ago
