Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
4 C Medical Technologies
Overview
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
Quick view →
Compensation
$75,000 - $95,000 / YEAR
Posted
6 days ago
Headlands Research
Coordinate all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. Manage subject visits, recruitment, data entry, and collaboration with investigators and sponsors.
$70,000 - $80,000 / YEAR
9 days ago
The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaborating with investigators and lab teams to maintain study integrity.
Salary not listed
The Clinical Research Coordinator manages all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. They are responsible for subject visits, accurate documentation, data entry, and maintaining effective communication with investigators and sponsors.
Coordinate all aspects of assigned clinical trials from site initiation to study close-out, ensuring compliance with study protocols and regulations. Manage subject recruitment, conduct visits, and maintain accurate documentation throughout the trial process.
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
20 days ago
Beth Israel Lahey Health
The Clinical Research Coordinator II is responsible for coordinating and administering multiple research studies, ensuring adherence to protocols and regulatory requirements. This role involves working closely with principal investigators and research staff, as well as interacting with study participants diagnosed with cardiovascular disease.
$19 - $31 / HOUR
1 month ago
Beverly Hills Oncology Me
The Clinical Research Coordinator serves as the primary coordinator for assigned studies, ensuring adherence to trial protocols and managing subject scheduling and visits. Responsibilities also include data management, patient recruitment, and collaboration with the clinical team.
$32 - $34 / HOUR
Alliance For MultiSpecialty Research LLC
Manages clinical research study tasks with a specialized focus on investigational product handling, administration, and subject safety. Coordinates trial activities in compliance with FDA regulations, GCP guidelines, and protocol-specific requirements.
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
IQVIA
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
The US Oncology Network
The Clinical Research Coordinator II is responsible for recruiting, screening, consenting, and enrolling patients in clinical trials while ensuring protocol compliance. They also coordinate patient care, maintain investigational drug accountability, and prepare study-related documentation.
$58,798 - $77,435 / YEAR
Peregrine Team
The Clinical Research Coordinator will manage daily clinical trial activities, including patient scheduling and regulatory compliance. They will also serve as a key liaison between investigators, sponsors, and patients while ensuring accurate data entry into EDC systems.
Flourish Research
The Clinical Research Coordinator assists investigators in executing clinical trials in accordance with study protocols and regulatory guidelines. Responsibilities include obtaining informed consent, performing lab draws, managing study documentation, and communicating with sponsors.
$24 - $26 / HOUR
Pinnacle Clinical Research
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.
K2 Staffing LLC
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and ongoing reporting. They also collaborate with clinical operations, sponsors, and IRBs to ensure audit-ready regulatory files and compliance with study protocols.
2 months ago
CenExel
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and performing data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
$20 - $22 / HOUR
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and close-out procedures. They also collaborate with clinical operations and sponsors to ensure audit-ready regulatory files and compliance with protocol requirements.
University of Colorado
The Regulatory Affairs Coordinator independently manages all IRB and regulatory processes for ophthalmology research studies. Responsibilities include preparing regulatory submissions, maintaining investigator site files, and ensuring compliance with institutional and federal regulations.
$59,995 - $87,761 / YEAR
Alcanza Clinical Research
The Clinical Research Registered Nurse ensures the execution of assigned studies and performs clinical procedures in compliance with study protocols and regulations. Responsibilities include patient screening, consent, follow-up visits, and documentation.
