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Systimmune
Overview
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
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Compensation
$90,000 - $130,000 / YEAR
Posted
9 days ago
Headlands Research
The Clinical Research Coordinator manages all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. They are responsible for subject visits, accurate documentation, data entry, and maintaining effective communication with investigators and sponsors.
Salary not listed
Duke Careers
This role involves managing all aspects of clinical research operations within the Anesthesiology Clinical Research Unit, including preparing FDA regulatory submissions, managing investigational products, and ensuring protocol compliance across various settings.
$59,829 - $99,960 / YEAR
12 days ago
Adams Clinical
The Clinician-Rater conducts structured clinical interviews, diagnostic evaluations, and standardized rating scales to assess psychiatric and neurological conditions. They work within a multidisciplinary team to determine participant eligibility and ensure high-quality data collection for clinical trials.
$90,000 - $120,000 / YEAR
13 days ago
The Clinician-Rater conducts structured clinical interviews, diagnostic evaluations, and neuropsychological assessments to support psychiatry and neurology clinical trials. They are responsible for determining participant eligibility and maintaining high-quality data collection in compliance with regulatory standards.
The Lead Study Therapist will provide support to participants throughout clinical trials and monitor dosing sessions in alignment with study protocols. They will also collaborate with the clinical team to ensure data quality and participant safety.
$60 - $70 / HOUR
ZOLL Medical Corporation
Provide administrative and operational support for clinical trials, including the maintenance of trial master files and regulatory documentation. Coordinate study activities, manage clinical data in CTMS and EDC systems, and ensure compliance with GCP and SOPs.
$28 - $32 / HOUR
1 month ago
Vanderbilt University Medical Center
Provide personalized nutrition counseling and medical nutrition therapy to children and families via telehealth for a clinical weight loss study. Collaborate with the research team to monitor intervention fidelity, manage documentation, and ensure adherence to study protocols.
$40 / HOUR
Epicrispr Biotechnologies
The role involves supporting the execution and oversight of clinical trials, including site management and on-site sample operations. The candidate will ensure compliance with GCP guidelines and collaborate with CROs to maintain data integrity and protocol adherence.
$115,000 - $121,000 / YEAR
Gastromed, LLC
The Sub-Investigator performs clinical assessments, ensures protocol adherence, and monitors subject safety throughout clinical trials. They collaborate with investigators and sponsors to maintain high-quality data and support patient recruitment efforts.
Deborah's Place
The Case Manager provides direct clinical services, including intake, assessment, and individual counseling to help tenants achieve housing and health goals. They also coordinate resources, manage crisis interventions, and maintain accurate tenant records in tracking databases.
Eli Lilly and Company
Provide scientific leadership to drive early discovery research in osteoporosis, including target evaluation and mechanism-based therapeutic strategies. Maintain a hands-on laboratory presence to execute in vitro and in vivo models for preclinical drug discovery and target validation.
$138,000 - $224,400 / 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
CenExel
The Quality Assurance Coordinator ensures data quality and participant safety by monitoring adherence to study protocols, SOPs, and federal regulations. They assist in developing QA programs, perform documentation reviews, and prepare the site for internal and external audits.
Mayo Clinic
The Clinical Research Coordinator will independently manage complex Alzheimer's disease research protocols, including participant recruitment, data monitoring, and regulatory compliance. The role also involves direct administration of neuropsychometric testing and cognitive assessments as a core responsibility.
$28 - $42 / HOUR
Perform advanced nerve conduction studies and provide specialized technical support for physician-performed electromyography in an academic clinical setting. Communicate relevant technical findings to support clinical decision-making and contribute to teaching and quality improvement efforts.
UCSF
The Clinical Research Coordinator will independently manage and execute research protocols for perioperative, critical care, and pain medicine studies. They are responsible for coordinating data collection and ensuring operations align with UCSF and regulatory agency policies.
World Relief
The Community Health Worker provides relationship-based support to clients, helping them navigate health and social service systems while addressing social drivers of health. They conduct outreach, facilitate health education workshops, and coordinate care in collaboration with healthcare providers and community partners.
$27 / HOUR
2 months ago
Loma Linda
The Coder 2-HIM performs ICD and CPT coding and abstracts data from medical records. They ensure coding accuracy and compliance with regulations while working with students and interns as needed.
Ardelyx
The Clinical Research Associate II provides sponsor oversight of assigned investigative sites, focusing on high-quality protocol execution and compliance with GCP and regulatory requirements. This role involves monitoring site performance through data review, supporting all phases of the clinical trial lifecycle, and ensuring timely collection and maintenance of essential regulatory documents.
$99,000 - $121,000 / YEAR
