Clinical Research Coordinator - Centennial - Nexus HR Services

    Nexus HR Services
    Nexus HR Services Centennial

    15 hours ago

    Description

    Clinical Research Coordinator - Centennial, CO

    Compensation: $50,000 - $70,000 Annually

    ** Overview: Nexus HR is seeking a Clinical Research Coordinator to join our team. In this pivotal role, you will maintain a neat and professional appearance, demonstrate commitment to serve at all times, uphold guidelines as set forth in the employee handbook, and maintain patient confidentiality at all times.**

    About the Job

    The Clinical Research Coordinator is involved in all aspects of clinical trials research from pre-study planning to study completion, and includes direct involvement in case management of study participants. Works under the supervision of the Principal Investigator and Site Manager.

    Duties and Responsibilities:

    • Own end-to-end management and execution of all clinical research activities
    • Independently conduct and complete study visits, including protocol review with the Principal Investigator
    • Lead patient recruitment and retention initiatives and support internal study marketing efforts
    • Ensure compliant informed consent before any study procedures
    • Review medical records and eligibility criteria with investigators or site leadership
    • Perform safety assessments (e.g., vitals, venipuncture, ECGs)
    • Create, maintain, and complete source documentation and regulatory binders
    • Schedule subjects, manage follow-up, and coordinate with physicians and sponsors
    • Collaborate with clinical teams to ensure protocol adherence and documentation accuracy
    • Complete CRFs and manage queries in a timely, compliant mannerCoordinate research operations across multiple studies, phases, and therapeutic areas
    • Complete and maintain training in ICH/GCP, HIPAA, SOPs, IATA, and other required technical skills
    • Understand Investigator and Site responsibilities under FDA, DHHS, and OHRP regulations
    • Knowledgeable of the drug development process (IND to NDA, IDE to PMA, Phases I–IV)
    • Comprehend and communicate informed consent elements per the Declaration of Helsinki
    • Understand IRB regulations and their role in clinical trials
    • Identify and report adverse and serious adverse events promptly
    • Participate in site initiation, monitoring, and closeout visits, as well as sponsor meetings
    • Engage in peer review of data quality
    • Adhere to IMMUNOe policies and procedures
    • Maintain regular attendance as an essential job function

    Qualifications :

    • Bachelor's degree in biology, chemistry, human sciences, or a related scientific field; relevant clinical experience may substitute
    • 2–5 years of healthcare and/or clinical research experienceCertification in the field (CCRC, CCRA, or CCRP) preferred
    • Strong attention to detail and organizational skills
    • Excellent written and verbal communication
    • Ability to manage multiple studies concurrently
    • Proficient in basic computer applications
    • Demonstrates honesty, integrity, and professionalism
    • Effective team player in a high-performance environment

    Benefits:

    • 401(k) and 401(k) matching
    • Health, dental, and vision insurance
    • Life and disability insurance (short-term and long-term)
    • Flexible spending accounts (FSA)
    • Health Savings Accounts (HSA)
    • Employee Assistance Program (EAP)
    • Paid time off (PTO) and holiday pay
    • Wellness programs
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