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M3USA
Overview
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
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Compensation
Salary not listed
Posted
17 days ago
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
$30 - $40 / HOUR
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the Investigator with participant screening, maintaining documentation, collecting and entering data, and overseeing other research staff.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
The Clinical Research Coordinator manages daily clinical trial activities, including screening participants and maintaining essential study documentation. They ensure all activities comply with research protocols, laws, and regulatory requirements while supporting the Principal Investigator.
$25 - $35 / HOUR
21 days ago
1 month ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with participant screening, maintaining documentation, and ensuring all activities comply with the research protocol and regulations.
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening study participants, maintaining documentation, and ensuring compliance with research protocols.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with screening, maintaining documentation, collecting and entering data, and mentoring junior staff.
TIDEWATER PHYSICIANS MULTISPECIALTY GROUP P C
The Clinical Research Coordinator manages the daily operations of clinical studies, including patient enrollment, protocol compliance, and data collection. They also handle laboratory specimens, maintain regulatory documentation, and coordinate with investigators and sponsors to ensure study success.
2 months ago
US Foot & Ankle Specialists
The Clinical Research Coordinator manages and conducts clinical research projects by leading trial operations, collecting data, and ensuring strict adherence to Foot and Ankle Specialists of the Mid-Atlantic (FASMA) Standard Operating Procedures (SOPs). Key duties include monitoring study activities for compliance, maintaining detailed study records, managing subject enrollment, and acting as a liaison between investigators, the IRB, CRO, and sponsor.
INSIGHT Surgical Hospital
The Clinical Research Coordinator Assistant supports the CRC, administrative staff, and principal investigators by overseeing clinical study details, ensuring compliance with regulations, and assisting with communications between sponsors and institutes. Key duties include performing study start-up tasks, executing recruitment plans, maintaining study documentation, collecting data, and performing technical study procedures like phlebotomy.
3 months ago
Rovia Clinical Research
This role involves managing the day-to-day operations of clinical studies, ensuring execution aligns with protocols, GCP, and SOPs, including coordinating startup activities, overseeing facility issues, and leading site meetings. Responsibilities also include monitoring enrollment progress, ensuring timely data entry into platforms like EDC, leading study visits, and providing guidance and training to site research staff.
$55,000 - $70,000 / YEAR
