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Mass General Brigham
Overview
This role supports research studies in Sleep and Circadian Disorders by instructing subjects, obtaining informed consent, collecting, organizing, and analyzing study data, and preparing regulatory documentation. Responsibilities also include creating REDCap surveys and databases, training personnel, and troubleshooting specialized data collection devices during various shifts.
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Compensation
$20 - $29 / HOUR
Posted
2 days ago
Mohawk Valley Health System
The Clinical Research Nurse facilitates and coordinates daily clinical trial activities, ensuring adherence to protocols and regulatory requirements. They work closely with the Principal Investigator to manage study documentation, participant recruitment, and data collection.
$75,000 - $115,000 / YEAR
4 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.
Salary not listed
6 days ago
Evolution Research Group
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.
9 days ago
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.
Lead and oversee clinical trials ensuring compliance with protocols and ethical guidelines. Provide leadership and mentorship to site staff while overseeing subject safety and trial conduct compliance.
$130 - $160 / HOUR
The Christ Hospital Health Network
The Clinical Research Coordinator supports the Principal Investigator by coordinating daily clinical trial activities and ensuring data integrity. They provide guidance on compliance, financial, and personnel aspects of the study to ensure human subject safety.
10 days ago
Advanced Psychiatric Group
The psychiatrist will conduct comprehensive psychiatric evaluations, create individualized treatment plans, and provide medication management. Additionally, they will serve as Principal Investigator for clinical trials, overseeing study conduct and ensuring regulatory compliance.
$300,000 / YEAR
13 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.
University of Massachusetts Medical School
The Research Associate provides operational support to the laboratory by performing defined research experiments under the direction of the Principal Investigator, ranging from basic tasks at Level I to independent project management and protocol development at Level IV. Responsibilities also include maintaining accurate records, assisting with data analysis, monitoring supplies, and ensuring compliance with all safety and institutional regulations.
21 days ago
The Research Associate provides operational support to the laboratory, performing research experiments focused on microbiota-metabolite-immune system crosstalk in the intestines using advanced techniques like flow cytometry, sequencing, and metabolomics. Responsibilities scale with rank, ranging from performing basic experiments and maintaining records to independently designing complex experiments, managing lab operations, and contributing to grant and manuscript writing.
The Research Associate provides operational support to the laboratory by performing defined research experiments under the direction of the Principal Investigator. Responsibilities scale with rank, ranging from basic experiment execution and data recording to independent complex experiment design, management of lab operations, and contribution to grant and manuscript writing.
$40,000 - $73,000
The Research Associate provides operational support to the laboratory by performing research experiments as defined by the Principal Investigator, ranging from basic tasks at Level I to independent design and management at Level IV. Responsibilities include data collection, analysis, protocol adherence, maintaining lab supplies, and ensuring compliance with safety regulations.
$40,000 - $45,000
The Research Nurse Coordinator is responsible for carrying out delegated tasks related to complex protocols testing investigational drugs and devices. They act as a liaison between various stakeholders to ensure good clinical practice standards throughout the study lifecycle.
$34 - $53 / HOUR
Tandem Intermediate LLC
The Clinical Research Nurse oversees daily study activities and ensures all procedures follow protocol guidelines. Responsibilities include collecting patient data, performing clinical tasks, and maintaining communication between investigators, sponsors, and patients.
Medical University of South Carolina
The Staff Scientist I will execute research activities focusing on animal procedures, behavioral studies (35%), and wet lab procedures like staining and microscopy (35%) related to neuroimmunology projects. Additional duties include scientific communication, reporting, and general laboratory support, training, and organization.
24 days ago
ALS
The coordinator plans and develops safety and efficacy research studies under the supervision of a Principal Investigator. They oversee day-to-day clinical activities, supervise research assistants, and manage study workflow and reporting.
25 days ago
Nira Medical
Provide specialized care for patients with movement disorders, including Parkinson's disease and dystonia, within an outpatient setting. Manage advanced therapeutics such as DBS programming and botulinum toxin injections while participating in clinical research trials.
Arensia Exploratory Medicine
Collaborate on clinical trials across various therapeutic areas, specifically in gastrointestinal, ophthalmology, and vascular surgery. Roles include serving as Principal Investigator or Sub-I, providing advisory support, monitoring, and protocol review.
