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Ann & Robert H. Lurie Children's Hospital of Chicago
Overview
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
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Compensation
$49,920 - $81,619 / YEAR
Posted
6 days ago
Evolution Research Group
The Clinical Research Coordinator manages the implementation of clinical trials, including subject screening, enrollment, and the administration of study procedures. They ensure all activities comply with FDA regulations, GCP guidelines, and company SOPs while maintaining accurate study documentation.
Salary not listed
9 days ago
The Research Assistant is responsible for assisting with clinical research studies, collecting and analyzing data, and ensuring strict adherence to study protocols and FDA regulations. They will also perform clinical tasks such as phlebotomy and ECGs while maintaining accurate study records and managing lab inventory.
Emory University
The Clinical Research Coordinator II manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, supervising specimen collection, and ensuring strict protocol compliance.
24 days ago
Kettering Health
The Clinical Research Coordinator I assists investigators in executing research trials by screening and enrolling subjects and ensuring protocol compliance. They are responsible for data reporting, adverse event tracking, and maintaining regulatory files in accordance with GCP guidelines.
28 days ago
CenExel
The Research Assistant provides direct support to Clinical Research Coordinators by managing patient charts, preparing visit materials, and performing data entry. They also conduct basic clinical assessments and maintain study-specific supplies while adhering to strict regulatory guidelines.
Lurie Children's Hospital
The coordinator manages the GROWTH study by handling regulatory documents, recruiting subjects, and collecting/processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
$46,280 - $75,670 / YEAR
29 days ago
Tufts Medicine
The Clinical Research Coordinator assists in planning and implementing cardiovascular clinical research studies, including participant recruitment, screening, and data collection. They are responsible for maintaining regulatory compliance, managing study documentation, and ensuring patient safety throughout the research process.
$47,924 - $59,895 / YEAR
This role involves assisting the Principal Investigator in planning and implementing clinical research studies, including participant recruitment, screening, and follow-up activities. Responsibilities also cover maintaining regulatory compliance, managing study documentation, performing basic lab activities, and coordinating data collection and query resolution.
Maine Eye Center
The coordinator assists the Principal Investigator in implementing clinical research studies, focusing on participant recruitment and eligibility screening. They are responsible for maintaining regulatory documentation, performing data entry, and ensuring compliance with FDA and IRB guidelines.
1 month ago
UCSF
The role involves supporting daily clinical trial operations with a primary focus on study data entry and coordination. Responsibilities include recruiting subjects, managing study documentation, and ensuring the collection and shipment of samples.
$32 - $39 / HOUR
Thermo Fisher Scientific
The Clinical Research Nurse conducts clinical trials by providing medical care to patients and ensuring adherence to FDA, GCP, and ICH regulations. Responsibilities include performing protocol procedures, managing patient documentation, and coordinating with site teams from study initiation to closeout.
Coordinates clinical research activities, including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing to ensure protocol adherence and accuracy.
The role involves supporting clinical trials primarily through study data entry and the coordination of active or follow-up trials. Responsibilities include recruiting subjects, gathering medical data, and preparing reports and protocols under the supervision of a manager.
$32 - $38 / HOUR
The coordinator manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, processing specimens, and ensuring strict protocol compliance.
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
The Pharmacy RN coordinates with the pharmacist to support clinical investigational drug trials, including the accurate dispensing of medication. They are responsible for monitoring pharmacy activities to ensure strict adherence to study protocols, FDA guidelines, and GCP standards.
$36 - $39 / HOUR
Pinnacle Clinical Research
The Clinical Research Coordinator manages daily clinical trial operations, including patient recruitment, screening, and study protocol execution. They ensure regulatory compliance, maintain accurate documentation, and collaborate with sponsors and medical staff to provide high-quality patient care.
The Clinical Research Coordinator manages daily clinical trial operations, including participant recruitment, screening, and study protocol adherence. They also ensure accurate documentation, regulatory compliance, and effective communication with sponsors and the research team.
2 months ago
