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University of Texas Medical Branch (UTMB)New
Overview
Provides professional nursing care for participants in oncology and hematology research studies while ensuring compliance with study protocols and federal regulations. Manages clinical study operations, including participant recruitment, informed consent, data collection, and regulatory documentation.
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Compensation
Salary not listed
Posted
New
Provides professional nursing care for participants in oncology and hematology research studies while ensuring compliance with study protocols and federal regulations. Manages clinical study operations, including participant recruitment, data collection, and regulatory documentation.
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
2 days ago
ICON plc
The intern will support clinical delivery by managing essential document collection, maintaining the Trial Master File, and ensuring timely data entry into CTMS. They will also assist with risk assessment, trial material tracking, and general clinical operations tasks.
$19 / HOUR
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data entry and site documentation.
Iterative Health
The Clinical Research Coordinator manages industry-sponsored clinical trials, including patient recruitment, visit coordination, and specimen processing. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and PIs.
3 days ago
The Clinical Research Coordinator manages industry-sponsored clinical trials, focusing on patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and investigators.
The Clinical Research Coordinator manages industry-sponsored clinical trials, including patient recruitment, visit coordination, and clinical procedures. They are responsible for maintaining study documentation, ensuring data integrity, and communicating with sponsors and investigators.
The Clinical Research Coordinator manages the daily activities of industry-sponsored clinical trials, including patient recruitment and visit coordination. They are responsible for clinical tasks like blood draws and ECGs, while ensuring strict adherence to study protocols and regulatory guidelines.
The CRC II manages industry-sponsored clinical trials, overseeing patient recruitment, study visits, and the collection of clinical data. They are responsible for maintaining high-quality documentation and coordinating communication between sponsors, CROs, and the Principal Investigator.
The CRC II manages industry-sponsored clinical trials by coordinating daily activities, leading patient recruitment, and conducting study visits. They are responsible for specimen processing, data entry into CTMS, and maintaining communication with sponsors and PIs.
The Clinical Research Coordinator II manages daily clinical trial activities, including protocol management, patient recruitment, and study visit coordination. They are responsible for ensuring data integrity, maintaining regulatory documentation, and serving as the primary point of contact for study participants.
The Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures like blood draws and IV administration. They also ensure data integrity, maintain study documentation, and act as the primary point of contact for study participants.
The Research Assistant supports clinical trial activities by assisting the study team with recruitment, screening, and protocol management. They are also responsible for maintaining study documentation, managing supplies, and ensuring compliance with regulatory and site policies.
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
Mohawk Valley Health System
The Clinical Research Nurse facilitates and coordinates daily clinical trial activities, ensuring adherence to protocols and regulatory requirements. They work closely with the Principal Investigator to manage study documentation, participant recruitment, and data collection.
$75,000 - $115,000 / YEAR
4 days ago
Avalo Therapeutics
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
7 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
10 days ago
Headlands Research
Support clinical trial delivery by preparing study documents, conducting patient procedures like vital signs and phlebotomy, and managing study data. Coordinate participant visits and ensure compliance with FDA and Good Clinical Practice guidelines.
