Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
AstraZeneca
Overview
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.
Quick view →
Compensation
$112,154 - $168,232 / YEAR
Posted
12 days ago
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.
Vitalief
Support Phase II–III oncology interventional clinical trials by screening, consenting, and enrolling patients. Coordinate care across medical teams and manage study documentation and patient records.
Salary not listed
22 days ago
Nemours Children's Health
The coordinator implements and manages clinical research studies within the Orthopedics Department, focusing on regulatory compliance and participant recruitment. Key duties include collecting study data, maintaining records, and interfacing with sponsors and auditors.
28 days ago
University of Southern California
The Protocol Coordinator manages clinical research trials by ensuring protocol compliance, coordinating patient eligibility, and monitoring adverse events. They act as a primary liaison between patients, physicians, and pharmaceutical sponsors to facilitate safe and accurate study execution.
$50 - $63 / HOUR
1 month ago
Pharmaron
The Clinical Regulatory Associate manages essential clinical trial documentation, IRB submissions, and study start-up activities. They ensure compliance with GCP, GLP, and internal procedures while supporting monitoring visits and study closeout activities.
$50,000 - $54,000 / YEAR
Tribe513 | The Onyx Group
The Clinical Research Coordinator is primarily responsible for conducting Phase II, III, and IV clinical trials according to international standards, overseeing assigned trials under the direction of the Primary Investigator and Site Lead. Key duties include managing the informed consent process, medical record review, protocol compliance, patient relations, and administration of investigational products.
2 months ago
Sansum Diabetes Research Institute
The Nurse Practitioner will serve as a Sub-Investigator, leading the clinical research team in medical aspects of trials under the Principal Investigator's supervision. Key duties include performing clinical research activities, ensuring protocol compliance, administering investigational medications, and providing direct care to study patients.
$70 - $100 / HOUR
3 months ago
University of Colorado
The primary responsibility is serving as a Clinical Research Coordinator, overseeing day-to-day operations for multiple clinical trials and ensuring alignment with established protocols. Key duties include subject recruitment, executing informed consent, performing study procedures like phlebotomy, and managing data entry into CRFs.
$48,446 - $60,000 / YEAR
The primary responsibility is to serve as a Clinical Research Coordinator supporting various research activities, overseeing day-to-day operations for multiple clinical trials, and ensuring protocol alignment. Key duties include subject recruitment, informed consent execution, performing study procedures like phlebotomy, and managing data entry into CRFs.
Hackensack Meridian Health
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials, participating in assessing, planning, implementing, and evaluating compliant patient care within those trials under the principal investigator's supervision. Key duties include assisting with trial preparation, managing regulatory submissions to the IRB, recruiting and educating patients, monitoring patient progress, and maintaining accurate documentation.
$111,925 / YEAR
4 months ago
Florida Digestive Health Specialists LLP
The primary duties involve screening, enrolling, and following study subjects while ensuring strict adherence to protocol and regulatory compliance, often managing a greater study workload and increased interaction with Sponsors and CROs.
$61,000 - $68,000 / YEAR
5 months ago
