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ICON plcNew
Overview
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.
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Compensation
$19 / HOUR
Posted
New
Iterative Health
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.
Salary not listed
2 days ago
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.
6 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
9 days ago
Headlands Research
Support clinical trials by preparing study documents, recruiting participants, and conducting patient-facing procedures like vital signs and phlebotomy. Manage study data entry in EDC and CTMS systems while ensuring compliance with FDA and GCP guidelines.
$22 - $27 / HOUR
American Oncology Network
Responsible for the implementation and management of clinical research studies, including patient coordination and protocol adherence. Tasks include managing study designs, ensuring data integrity, and maintaining regulatory compliance under the supervision of a Principal Investigator.
$20 - $35 / HOUR
11 days ago
AstraZeneca
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for study sites, driving performance, resolving issues, and ensuring data quality through monitoring visits and source data review.
$112,154 - $168,232 / YEAR
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for sites, driving performance, resolving study-related issues, and managing study supplies.
American Clinical Research Services Opco LLC
The Clinical Research Coordinator manages clinical trials by overseeing subject recruitment, dosing, and data collection while ensuring regulatory compliance. They collaborate with investigators to maintain study documentation and monitor participant progress throughout the trial.
$50,000 - $67,000 / YEAR
13 days ago
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.
14 days ago
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 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 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 Senior Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures. They also ensure accurate data entry, maintain study documentation, and coordinate with sponsors and investigators to meet enrollment targets.
University of California, Irvine
Coordinate and manage Phase I-IV cancer-related clinical trials, ensuring adherence to GCP, SOPs, and university policies. Act as a liaison between sponsors, regulatory agencies, and the research team while managing patient recruitment and data collection.
15 days ago
