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IQVIA
Overview
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
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Compensation
$71,900 - $169,300 / YEAR
Posted
9 days ago
Headlands Research
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
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 data integrity, and overseeing drug accountability.
17 days ago
University of Virginia
The Clinical Research Coordinator will support day-to-day operations of multiple clinical trials in the NICU, including subject recruitment, screening, and enrollment. They will also maintain accurate study documentation and assist with data collection and specimen processing while ensuring protocol adherence.
23 days ago
Medical University of South Carolina
The Recruitment Coordinator manages the day-to-day identification and enrollment of research subjects across multiple disease areas. They collaborate with investigators to meet recruitment goals and handle clinical tasks such as obtaining informed consent and processing laboratory specimens.
$45,300 - $77,000 / YEAR
1 month ago
CentraState Healthcare System
The Research Nurse oversees and directs the clinical course of research participants in clinical trials under the direction of the principal investigator or manager, ensuring strict adherence to local and federal laws and regulations. Key duties involve study implementation, subject recruitment, enrollment, accurate documentation, and acting as the liaison between the sponsor and physician regarding protocol activities.
$48 - $82 / HOUR
UVA Health
The Clinical Research Coordinator will support day-to-day operations of multiple clinical trials in the NICU, including subject recruitment, screening, and enrollment. They will also maintain accurate study documentation and coordinate with investigators and clinical staff to ensure protocol adherence.
Platinum Dermatology Partners LLC
The Clinical Research Coordinator is responsible for managing administrative aspects of clinical trials, including subject recruitment, screening, and enrollment. They also assist physicians with clinical procedures and ensure all study activities comply with FDA, GCP, and IRB guidelines.
$30 - $33 / HOUR
Perform site monitoring and management to ensure study compliance with protocols, regulations, and sponsor requirements. Manage study progress, including regulatory submissions, recruitment tracking, and data integrity verification.
$64,000 - $189,000 / YEAR
Sago
The Research Project Interviewer supports study execution by conducting subject interviews, obtaining informed consent, and managing study visits. They also ensure all documentation complies with regulatory requirements and collaborate with the clinical project management team.
$15 / HOUR
University of Colorado
The Clinical Research Coordinator oversees day-to-day operations of clinical trials, including subject recruitment, data collection, and protocol adherence. They collaborate with investigators and hospital staff to ensure all research procedures are documented and compliant with regulatory standards.
$49,899 - $58,705 / YEAR
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
United Urology Group
The Research Coordinator will screen, enroll, and monitor study subjects for clinical trials while ensuring strict adherence to protocols and regulatory standards. Responsibilities include managing study documentation, coordinating with investigators, and performing clinical procedures such as venipuncture and specimen collection.
DERMCARE MANAGEMENT LLC
The Clinical Research Coordinator is responsible for overseeing the smooth operation of clinical trials by performing clinic visits, administering questionnaires, and ensuring adherence to GCP and FDA regulations. They also manage investigational medication, maintain detailed study records, and facilitate communication between investigators, sponsors, and research subjects.
The Clinical Research Coordinator is responsible for overseeing clinical trials, performing visit procedures such as phlebotomy and EKGs, and ensuring adherence to GCP and FDA regulations. They also manage investigational medication, maintain detailed study records, and engage with research subjects and sponsors.
The Clinical Research Associate is responsible for performing site monitoring visits to ensure study protocol adherence and regulatory compliance. They also manage site recruitment plans, maintain study documentation, and oversee data integrity throughout the clinical trial process.
$87,200 - $182,000 / YEAR
Profound Research
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols and regulations. They also mentor staff and ensure accurate documentation and reporting of adverse events.
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols. They also mentor staff and ensure accurate documentation and reporting of adverse events.
The Clinical Research Coordinator manages all clinical trial activities in compliance with study protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical research operations.
The Senior CRA is responsible for monitoring and managing clinical sites to ensure strict adherence to study protocols, regulatory requirements, and sponsor expectations. They will conduct various site visits, facilitate subject recruitment, and maintain essential study documentation to ensure high-quality clinical research data.
$87,200 - $169,300 / YEAR
