Clinical Research Coordinator (RN/LPN) jobs in United States
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Call Quest Solution · 1 day ago

Clinical Research Coordinator (RN/LPN)

Call Quest Solution is seeking a Clinical Research Coordinator to oversee multiple active clinical trials with a focus on patient safety and protocol compliance. This role involves managing site logistics, supporting vendor coordination, and ensuring regulatory compliance throughout the study lifecycle.

Staffing & Recruiting

Responsibilities

Conduct clinical studies in compliance with FDA regulations, GCP, and ICH guidelines
Ensure patient safety and quality of care at all times
Coordinate and schedule subject visits within protocol-defined windows
Perform study procedures, including:
Informed consent
Screening and enrollment
Vital signs, ECGs, height/weight measurements
Pregnancy testing and other protocol-defined procedures
Accurately document patient data in required study systems and forms (CRFs, EDC)
Maintain and update source documents and patient records
Manage investigational product (IP) accountability, when required
Ensure IRB approvals are obtained prior to study initiation and maintained throughout the study
Identify and report suspected protocol deviations or non-compliance
Participate in site initiation visits (SIVs) and protocol training sessions
Support patient outreach activities, including scheduling, follow-ups, and result notifications
Promote patient engagement and retention through strong relationship-building
Adhere to company policies, SOPs, and clinical operating procedures
Assist with facility upkeep and proper waste disposal per regulatory standards

Qualification

Clinical research operationsGCPSOPsRegulatory complianceInformed consent processPatient safetyAnalytical skillsCommunication skillsBasic computer applicationsEnglish fluencyAttention to detailProblem-solving skillsOrganizational skillsTeam collaboration

Required

Bachelor's degree or equivalent in a clinical or medical-related field
Active nursing license required (RN, LPN, or LVN), registered with the local healthcare authority
Minimum 2+ years of relevant clinical research or comparable experience
Strong understanding of clinical research operations, including GCP and SOPs
Informed consent process
Safety monitoring and regulatory compliance
Ability to work independently with high attention to detail
Strong analytical, problem-solving, and decision-making skills
Demonstrated discretion and sound judgment in handling sensitive information
Effective communication and interpersonal skills
Strong organizational and time-management abilities
Proficiency with basic computer applications and clinical systems
Ability to collaborate effectively in a team-based clinical environment

Preferred

English fluency preferred

Company

Call Quest Solution

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At Call Quest Solutions, we believe great companies are built by great people.

Funding

Current Stage
Growth Stage
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