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Iterative Health
Overview
The Research Assistant supports clinical trial activities by assisting the study team with recruitment, screening, and protocol management. They are also responsible for maintaining study documentation, managing supplies, and ensuring compliance with regulatory and site policies.
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Compensation
Salary not listed
Posted
3 days ago
Evolution Research Group
The Sub-Investigator acts as the secondary physician overseeing clinical trials, ensuring protocol adherence and regulatory compliance at the research site. They are responsible for managing subject care, documenting study procedures, and maintaining the integrity of clinical data.
$100,000 - $150,000 / YEAR
9 days ago
Headlands Research
Support clinical trial execution by conducting patient recruitment through outbound calls and assisting with subject screening and enrollment. Collect vital signs and document study data in electronic systems while ensuring compliance with study protocols.
Mass General Brigham
The Co-op Assistant supports clinical research studies by developing patient recruitment strategies and managing data collection. They are also responsible for processing blood samples, maintaining regulatory binders, and performing administrative scheduling tasks.
$18 - $24 / HOUR
29 days ago
Eye Care Partners Career Opportunities
The Clinical Research Coordinator oversees study protocols, ensures compliance with regulatory boards, and manages site-specific research activities. They are responsible for patient recruitment, data collection, and maintaining accurate documentation for clinical trials.
1 month ago
Arizona Liver Health
The coordinator is responsible for identifying and pre-screening potential participants for clinical trials to meet enrollment goals. They serve as an educational resource for patients and collaborate with investigators and research staff to manage the recruitment pipeline.
$60,000 - $85,000 / YEAR
Lurie Children's Hospital
The role supports clinical and behavioral health research projects by assisting with study implementation, regulatory documentation, and IRB submissions. Responsibilities also include participant recruitment, data collection via REDCap, specimen processing, and maintaining study-specific records.
$46,280 - $75,670 / YEAR
McKesson
The Enrollment Research Nurse is responsible for screening and enrolling oncology patients into clinical trials while ensuring strict protocol compliance. They will document patient data, manage study medication orders, and coordinate with physicians to maintain accurate clinical trial records.
University of Colorado
The professional will assist with the day-to-day operations of clinical trials, including subject recruitment, data collection, and ensuring regulatory compliance. They will also educate potential subjects, manage study schedules, and perform laboratory duties such as processing and cryopreserving human blood.
$49,889 - $63,472 / YEAR
The professional will assist with the day-to-day operations of clinical trials, including subject recruitment, data collection, and ensuring regulatory compliance. They will also perform informed consent processes and coordinate study logistics with clinical staff.
Montefiore Health System
The Research Associate oversees multiple clinical trials, ensuring adherence to study protocols, regulatory requirements, and seamless daily trial activities. They coordinate team members, manage patient recruitment and assessments, and handle IRB documentation and billing processes.
Alcanza Clinical Research
The Research Assistant supports clinical research coordinators and investigators by performing clinical, laboratory, and administrative tasks according to study protocols. Responsibilities include patient screening, data entry, vital sign collection, and maintaining study documentation in compliance with regulatory standards.
ICON plc
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing documentation, and overseeing drug accountability.
The Research Associate supports the clinical research team by managing patient data, ensuring protocol compliance, and assisting with recruitment and informed consent processes. They are responsible for maintaining subject files, handling clinical specimens, and coordinating monitor visits under supervision.
$56,000 - $70,000 / YEAR
US Fertility
The Research Coordinator will manage all aspects of fertility-related clinical trials, including participant recruitment, informed consent, and data collection. They will also serve as the primary point of contact for patients and investigators while ensuring compliance with regulatory standards.
2 months ago
The Patient Liaison supports onsite patient recruitment by executing pre-qualification, pre-screening, and scheduling activities to ensure efficient enrollment into active studies. Key duties involve evaluating subject eligibility, managing patient follow-up communication, monitoring screening schedules, and driving screening numbers to meet established recruitment goals.
CenExel
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties involve creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution.
3 months ago
The Recruitment Specialist I is responsible for recruiting patients via telephone and assisting with recruitment programs to boost referrals for various clinical research trials. Essential duties include maintaining professional relationships with potential participants and performing initial telephone screenings.
Medpace, Inc.
The coordinator will implement various recruitment strategies for clinical research studies and collaborate with the Clinical Research Associate to discuss enrollment targets. Responsibilities also include developing recruitment plans, tracking media referrals and enrollment progress using internal systems, and updating study-specific social media sites.
The primary duties involve recruiting patients via telephone and assisting with recruitment programs to boost participant referrals for various clinical research trials. This includes performing initial telephone screenings and scheduling appointments in Clinical Conductor.
$20 - $23 / HOUR
4 months ago
