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OhioHealth
Overview
Provides coordination and administrative support for clinical trials, including data entry, specimen processing, and regulatory documentation. Assists research staff with IRB submissions, patient screening, and maintaining study records to ensure operational efficiency.
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Compensation
Salary not listed
Posted
5 days ago
Evolution Research Group
The role supports the Regulatory Manager in meeting submission targets by preparing and maintaining regulatory documents for sponsors and IRBs. Responsibilities include managing study logs, filing correspondence, and ensuring compliance with GCP and HIPAA guidelines.
$20 - $28 / HOUR
6 days ago
LCMC Health
The role manages regulatory documents and submissions to pharmaceutical sponsors, IRBs, and CROs to implement clinical trials. It also involves coordinating audits, performing quality assurance, and mentoring junior staff members.
8 days ago
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.
10 days ago
Mangrove Management Partners
Provides administrative and regulatory support for vascular clinical trials, including maintaining investigator documentation and IRB submissions. Manages staff training compliance, trial master files, and data transcription into EDC systems.
$60,000 - $65,000 / YEAR
12 days ago
Children's Mercy KC
Assists in the preparation and distribution of medications while coordinating quality assurance and regulatory compliance for sterile products. Conducts internal pharmacy audits and provides staff education on medication preparation and specialized programs.
$23 / HOUR
15 days ago
IRONWOOD PHYSICIANS,P.C.
Responsible for the timely submission and maintenance of accurate regulatory documents to pharmaceutical sponsors, IRBs, and contract research organizations. Oversees study initiation, monitoring, and closeout visits while ensuring compliance with federal regulations and international guidelines.
16 days ago
Duke Careers
The Regulatory Coordinator will manage regulatory operations for complex oncology studies, ensuring compliance and audit readiness. This includes preparing and submitting necessary documentation and coordinating study management activities.
$59,829 - $99,960 / YEAR
OneOncology
The Research Regulatory Coordinator manages regulatory files, IRB submissions, and essential documentation for clinical trials. They coordinate with sponsors and investigators to ensure compliance with regulatory best practices and safety reporting.
Orlando Health
The Pharmacy Regulatory Compliance Specialist ensures compliance with pharmacy regulations and oversees inspections and documentation related to medication safety. They also coordinate education and competency assessments for pharmacy personnel and manage the Continuous Quality Improvement program.
17 days ago
HR Anew
The role focuses on the operational execution of clinical trials, including participant coordination, visit preparation, and specimen collection. It also involves managing study data in EDC systems and maintaining accurate source documentation.
$45,000 - $55,000 / YEAR
The role focuses on the operational execution of clinical trials, including participant coordination, visit preparation, and specimen collection. Responsibilities also include entering study data into EDC systems and maintaining accurate source documentation.
INTERCOASTAL MEDICAL GROUP
The Regulatory Specialist manages research regulatory files and handles IRB submissions and study start-up/close-out documentation. They also coordinate with physicians and research managers while assisting with monitoring visits.
$22 - $28 / HOUR
22 days ago
Hygea Healthcare, Inc.
Provide individual, group, and family counseling to support individuals recovering from substance use disorders. Conduct trauma-informed assessments using ASAM criteria and maintain individualized treatment plans to promote long-term recovery.
24 days ago
The US Oncology Network
Responsible for managing research regulatory and administrative activities for clinical trials, including site qualification and document management. Collaborates with investigators and central operations to ensure compliance with SOPs, GCP, and federal regulations.
26 days ago
Medical University of South Carolina
The coordinator manages pre-award grant processes, including budget development and proposal submission. They also ensure regulatory compliance by managing IRB documentation and adhering to FDA and GCP requirements.
$37,200 - $59,500 / YEAR
1 month ago
Nationwide Children's Hospital
Assists with administrative components to ensure regulatory compliance for clinical research projects, including maintaining study binders and files. Prepares and submits IRB documents while ensuring accuracy across regulatory and grant systems.
Assists with administrative components to ensure regulatory compliance for clinical research projects. Responsibilities include maintaining study binders, submitting IRB documents, and collecting investigator credentials.
WakeMed Health & Hospitals
Performs routine and specialized laboratory tests to assist in disease diagnosis and treatment while maintaining laboratory equipment and supplies. Trains new staff and assumes responsibility for specific laboratory projects such as quality control and regulatory compliance.
Performs routine and specialized laboratory tests while evaluating and reporting patient results using independent judgment. Assists in the maintenance of laboratory equipment, quality control procedures, and the training of new staff members.
