Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Phoenix
Arizona
1452 live openings
Philadelphia
Pennsylvania
1366 live openings
Atlanta
Georgia
1347 live openings
Indianapolis
Indiana
Legal
VitalHires helps educators discover verified school and district opportunities. Confirm compensation, credentials, and deadlines on the official hiring site before applying.
Nevada System of Higher Education
Overview
The Research Assistant will recruit and enroll patients for clinical trials while ensuring adherence to all local, state, and federal research regulations. Responsibilities also include maintaining accurate study documentation, processing lab specimens, and assisting with IRB submissions and on-site sponsor visits.
Quick view →
Compensation
$19 - $27 / HOUR
Posted
8 days ago
Bristol Myers Squibb
The Associate Scientist is responsible for collecting, processing, and preparing tissue specimens for microscopic examination in support of toxicologic nonclinical studies. Key duties include performing necropsies, operating histology equipment, and serving as a study coordinator to ensure GLP compliance.
$86,670 - $105,029 / YEAR
9 days ago
NYU Langone Health
The Clinical Research Coordinator coordinates Endocrine clinical research studies from planning to completion, ensuring compliance with study protocols. Responsibilities include scheduling participants, preparing for study visits, and acting as the primary contact for bio-specimen collections.
$70,482 - $75,000 / YEAR
21 days ago
Cedars-Sinai
The Clinical Research Associate I will assist in coordinating and implementing non-complex research studies, including tasks such as data collection, scheduling participants, and ensuring compliance with guidelines. The role involves supporting supervising staff with regulatory submissions and maintaining research practices.
Salary not listed
Children's Hospital of Philadelphia
The Clinical Research Coordinator II coordinates all clinical research activities within the scope of clinical research protocols, managing day-to-day activities under the guidance of the Principal Investigator. Responsibilities include adhering to protocols, participating in the informed consent process, and ensuring patient safety.
$56,890 - $71,110 / YEAR
22 days ago
University of Massachusetts Medical School
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling study visits, and ensuring compliance with protocols.
23 days ago
UVA Health
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring high-quality data collection and protocol compliance. Collaborate with multidisciplinary teams to manage study visits, maintain accurate documentation, and process laboratory specimens.
$33 - $91,500 / HOUR
University of Miami
The Clinical Research Support Specialist assists in the recruitment, screening, and enrollment of study participants while managing data collection and regulatory documentation. They also conduct community outreach, schedule research visits, and maintain consistent communication with participants to ensure study adherence.
24 days ago
Sanford Health
As a Registered Nurse Clinical Research Coordinator, you will manage key components of study operations, including outreach, patient recruitment, and coordinating tests and procedures. You will engage directly with patients and research teams to support each step of the research process.
$28 - $44 / HOUR
25 days ago
M3USA
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.
1 month ago
The Clinical Research Coordinator manages study protocols, including patient screening, informed consent, and data collection. They ensure compliance with FDA and IRB regulations while maintaining accurate source documentation and reporting study progress.
$24 - $40 / HOUR
Lurie Children's Hospital
The Behavioral Research Coordinator II manages research projects, including study start-up, protocol coordination, and regulatory compliance. They also conduct research visits, facilitate behavioral interventions, and perform data analysis under the supervision of the Principal Investigator.
$49,920 - $81,619 / YEAR
Hospital for Special Surgery
The Research Assistant will support clinical research operations by assisting with patient recruitment, informed consent, and study visit coordination. They are also responsible for accurate data collection, regulatory submissions, and the safe handling of biospecimens.
$23 - $36 / HOUR
Emory University
The Clinical Research Coordinator II manages research project databases, develops study-related documentation, and ensures compliance with research protocols. They also interface with research participants to determine eligibility, obtain consent, and coordinate study procedures.
Johns Hopkins University
The Senior Research Nurse coordinates and implements clinical trials within the oncology research program, ensuring protocol compliance and subject safety. They manage project documentation, oversee data collection, and provide education to patients and staff throughout the research process.
$75,100 - $131,700 / YEAR
Revival Research Institute, LLC
The Clinical Research Coordinator will manage multiple studies, including participant screening, recruitment, and enrollment. They are also responsible for collecting and processing research specimens, maintaining source documents, and assisting with regulatory document preparation.
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
The RN Clinical Research Coordinator will coordinate patient visits and assist with lab orders and screenings for neuro and vascular clinical research trials. This role involves managing complex components of clinical trials and ensuring compliance with research protocols.
PAVIR
The Clinical Research Assistant will manage the administrative and clinical aspects of multiple clinical trials, including patient recruitment, enrollment, and protocol adherence. They will also coordinate regulatory submissions, maintain study documentation, and facilitate monitoring visits to ensure scientific integrity.
2 months ago
Northwell
The role involves facilitating participant recruitment and providing comprehensive support throughout the study process. Additionally, the fellow will manage study materials, compile findings, and ensure adherence to regulatory guidelines and project timelines.
$80,000 / YEAR
