Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
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.
Quick view →
Compensation
$37,200 - $59,500 / YEAR
Posted
New
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.
Salary not listed
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
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.
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
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.
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.
The coordinator is responsible for conducting clinical research studies, obtaining informed consent, and organizing study information. They also assist in preparing and submitting grant applications and IRB documentation.
The coordinator conducts and assists in clinical research studies under the supervision of senior staff. Key duties include obtaining informed consent, organizing study information, and assisting with grant and IRB submissions.
University of Rochester
Coordinates administrative activities for multi-site clinical research studies, including participant recruitment and consent. Manages study visits, ensures regulatory compliance, and assists in disseminating research findings through publications.
$21 - $30 / HOUR
Heluna Health
The Research Coordinator manages day-to-day operations for a NIDA-funded study, including participant recruitment, consent, and data collection. They serve as the primary liaison between the Syringe Services Program and the Lead Study Team to ensure protocol compliance.
Johns Hopkins University
The coordinator will administratively manage clinical protocol implementation and ensure the logistical execution of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating submissions to the Institutional Review Board.
$17 - $30 / HOUR
University of Oklahoma
Coordinate multiple cancer outcomes research protocols, including participant enrollment and data management using REDCap and OnCore. Collaborate with principal investigators and the IRB to develop protocols and contribute to manuscript development.
Assists in clinical research studies by obtaining informed consent and organizing study information. Supports the preparation of grant applications and documents for the Institutional Review Board and Grants and Contracts Office.
$21 - $35 / HOUR
The coordinator manages daily clinical research activities, including obtaining informed consent and organizing study information. They also assist in preparing grant applications and regulatory documents for the Institutional Review Board.
