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Medical University of South CarolinaNew
Overview
The incumbent will coordinate the recruitment, screening, and enrollment of research participants while collecting psychological and biological data. They are also responsible for maintaining regulatory documentation and providing administrative support for grant proposals and publications.
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Compensation
$37,200 - $59,500 / YEAR
Posted
New
University of Iowa
Manage and support clinical trial regulatory activities for the Pediatric Department, including IRB submissions and documentation. Act as a back-up study coordinator to assist with subject visits, data entry, and protocol execution.
Salary not listed
3 days ago
Ascension
Coordinate administrative and clinical aspects of multiple oncology research projects, including participant recruitment and monitoring. Collaborate with investigators and sponsors to ensure protocol compliance and manage IRB documentation and audits.
4 days ago
Mount Sinai Health System
The coordinator is responsible for conducting clinical research studies, obtaining informed consent, and organizing study information. They also assist in the preparation and submission of grant applications and IRB documents.
$17 - $41 / HOUR
7 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.
9 days ago
Baylor Scott & White Health
The Research Nurse II coordinates clinical trials from setup to closure, ensuring adherence to federal and institutional guidelines. Key duties include screening patients for eligibility, managing informed consent, and collaborating with Principal Investigators and pharmacy staff.
10 days ago
Sarasota Memorial Health Care System
Responsible for the timely and accurate administration of regulatory compliance for clinical research, including processing Human Research Protection Program and IRB documentation. The role involves informing leadership and staff regarding the regulatory status of clinical trials.
11 days ago
University of Massachusetts Medical School
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
21 days ago
Southcoast Health System, Inc.
Coordinate all activities related to clinical trials, including patient screening, follow-up, and correspondence with the Institutional Review Board and sponsors. Manage trial implementation, budget negotiations, and ensure strict adherence to federal and institutional guidelines for human subject research.
$57,554 - $96,762 / YEAR
23 days ago
UCSF
The coordinator executes and manages research protocols for patients with Parkinson's and other movement disorders. Key duties include collecting research data, managing regulatory documents, and coordinating complex clinic visits.
$38 / HOUR
25 days ago
The coordinator assists in daily clinical research activities, including obtaining informed consent and organizing study information. They also help prepare grant applications and documents for the Institutional Review Board and Grants and Contracts Office.
27 days ago
Creighton University
The coordinator independently manages the clinical course of research participants and performs required tests and data collection according to study protocols. They are also responsible for maintaining accurate case report forms and reporting regulatory issues to the Institutional Review Board.
The coordinator assists with daily clinical research activities, including obtaining informed consent and organizing study information. They also help prepare grant applications and documents for the Institutional Review Board and Grants and Contracts Office.
28 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.
University of Florida
Provide direct clinical care and case management for pediatric, adolescent, and adult patients with infectious diseases and HIV. Manage research protocol compliance, patient enrollment, and coordinate care within a multi-disciplinary medical clinic.
$115,000 - $130,000 / YEAR
Children's Healthcare of Atlanta
The Research Pharmacist manages investigational pharmaceutical care by evaluating and implementing research drug protocols. Responsibilities include the procurement, storage, and dispensing of study medications while ensuring compliance with state and federal regulations.
29 days ago
Tufts Medicine
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.
$47,924 - $59,895 / YEAR
Medical University of South Carolina
The coordinator manages pre-award grant processes, including budget development and proposal submission. They also ensure regulatory compliance by managing IRB documentation and adhering to FDA and GCP requirements.
1 month ago
Erlanger Health System
Provides administrative and clinical support for research studies, including patient scheduling, specimen collection, and data entry. Manages regulatory documentation and coordinates with various hospital departments to ensure protocol compliance.
The Research Coordinator I provides administrative and clinical support for research studies, including patient care and specimen collection. They are responsible for maintaining study records, managing databases, and ensuring compliance with IRB requirements.
