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Evolution Research Group
Overview
The Clinical Research Coordinator manages the implementation of clinical trials, ensuring adherence to protocols and regulatory requirements. They are responsible for screening and enrolling subjects, maintaining accurate study records, and reporting adverse events under the direction of the Principal Investigator.
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Compensation
Salary not listed
Posted
9 days ago
Headlands Research
The Clinical Rater administers and evaluates study-specific clinical scales and psychometric tests to assess adult patients in clinical trials. They ensure data collection aligns with study protocols and communicate effectively with various stakeholders.
Tandem Intermediate LLC
The Clinical Research Nurse oversees daily study activities and ensures all procedures follow protocol guidelines. Responsibilities include collecting patient data, performing clinical tasks, and maintaining communication between investigators, sponsors, and patients.
21 days ago
Inotiv
Responsible for the daily care, husbandry, and well-being of laboratory animals in compliance with SOPs and federal regulations. Duties include facility upkeep, monitoring animal health, and assisting with in-life study conduct and data collection.
$18 - $20 / HOUR
24 days ago
University of Virginia
Perform surveillance and monitoring of results and adverse events for clinical research studies within the Health Sciences Center. Provide education and consultation to healthcare personnel, patients, and faculty while assisting Principal Investigators during regulatory audits.
$33 / HOUR
28 days ago
K2 Staffing LLC
The Pharmacy Specialist manages the receipt, storage, and dispensing of study drugs while ensuring strict compliance with FDA regulations and study protocols. They also develop training programs for clinic staff and coordinate study close-out procedures with sponsors.
1 month ago
The Geneva Foundation
The Research Coordinator oversees and administers research study activities, including project planning, regulatory compliance, and protocol implementation. They also manage data collection systems, recruit research subjects, and coordinate technical support staff to ensure study objectives are met.
$60,000 - $65,000 / 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.
Mass General Brigham
The Clinical Research Coordinator will assist with clinical research studies by recruiting and consenting patients, collecting data, and maintaining study records. They will also serve as a liaison between patients and physicians while ensuring compliance with IRB protocols and study guidelines.
$24 - $39 / HOUR
Fortrea
The Telemetry Technician will provide continuous cardiac monitoring and clinical support for research participants in Phase I clinical trials. Responsibilities include interpreting telemetry data, performing ECGs, documenting vital signs, and ensuring study protocol compliance.
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.
Flourish Research
The Clinical Research Coordinator assists investigators in executing clinical trials in accordance with study protocols and regulatory guidelines. Responsibilities include obtaining informed consent, performing lab draws, managing study documentation, and communicating with sponsors.
$24 - $26 / HOUR
The Clinical Research Coordinator manages all clinical trial activities in compliance with research protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical trial conduct.
CenExel
The technician is responsible for conducting diagnostic testing, maintaining laboratory logs, and ensuring strict adherence to clinical research protocols and regulatory standards. They also assist in site preparation, sample management, and the organization of study supplies.
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and performing data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
$20 - $22 / HOUR
2 months ago
Worldwide Clinical Trials
The Paramedic oversees study procedures, performs technical and laboratory tasks, and provides medical coverage for subjects in-house. They also act as a primary contact for subjects and supervise technical staff in the absence of a supervisor.
The Pharmacy Specialist assists in drug management and compliance, ensuring proper handling and documentation of drug products. They also support quality assurance and training for clinic staff interacting with the pharmacy.
The Licensed Vocational Nurse coordinates with the Pharmacist to support clinical drug trials, providing nursing care and managing study documentation. Responsibilities include monitoring study participants, ensuring compliance with protocols, and maintaining communication with sponsors.
$29 - $30 / HOUR
Alcanza Clinical Research
The Clinical Research Registered Nurse ensures the execution of assigned studies and performs clinical procedures in compliance with study protocols and regulations. Responsibilities include patient screening, consent, follow-up visits, and documentation.
