Clinical Research Coordinator

S

Serv Recruitment Agency

Clinical Research Coordinator

Albuquerque, NM
Full Time
Paid
  • Responsibilities

    Southwest Women's Oncology Team (SWWO) is rapidly growing and looking for a dedicated and driven Clinical Research Coordinator to join their high-performance team. SWWO's integrated group of healthcare professionals provides expert, compassionate care and delivers curative outcomes for their patients. With a focus on advanced surgical techniques, clinical trials, and patient advocacy, SWWO is uniquely positioned as a private practice with state-of-the-art resources and strong institutional partnerships.

    This Role includes:

    • Supervising and leading a team of clinical research coordinators.
    • Ensuring staff is trained in policies and procedures.
    • Monitoring time and attendance for staff.
    • Coordinating site qualification, study startup visits, interim monitoring visits, and study close-out visits.
    • Organizing and conducting training for research staff on protocols and research procedures.
    • Ensuring accurate clinical trial billing and study receivables in collaboration with the clinical trial finance office.
    • Monitoring study activities to ensure compliance with protocols and regulatory policies.
    • Assessing eligibility of potential subjects and overseeing informed consent processes.
    • Overseeing protocol compliance, adverse event reporting, and investigational product accountability.
    • Preparing study-related documentation, including protocol worksheets, adverse event reports, and progress reports.
    • Collaborating with pharmacy and nursing staff for protocols requiring IV medications.
    • Performing biospecimen processing, data entry, and shipping research specimens in accordance with standards.
    • Able to obtain vitals, administer 12 Lead ECG, draw blood, process tissue and blood specimens, and ship research specimens in accordance with GLP & IATA standards.
    • Maintain excellent report with PI, Sub-I, Nursing Staff, and Patients

    Qualifications:

    • Strong leadership skills with the ability to effectively communicate and create a high-performance environment.
    • Knowledge of biological and medical terminology.
    • Understanding of administration and management principles.
    • Ability to coordinate therapeutic phase II-IV drug or device trials.
    • Be adaptable, flexible, and able to change as required.

    Education and Experience:

    • Allied Health Certification with 5 years of experience as a CRC, including 1 year coordinating complex oncology trials.

    • BA/BS in a basic or health science field with 3 years of CRC experience, including 1 year coordinating complex oncology trials.

    • MA/MS in a basic or health science field with 2 years of CRC experience, including 1 year coordinating complex oncology trials.

    • Plan to obtain or currently hold CCRP/CCRC certification within 1 year of hire.

    • Clinical experience across multiple therapeutic areas, including oncology.

    Physical Requirements:

    • Prolonged periods of sitting and working on a computer.
    • Ability to lift up to 15 pounds as needed.

    Our Dream Teammate will have access to:

    • Competitive Salary
    • Excellent Benefits: Medical, dental, vision, PTO, and 401K
    • High-Performance Concierge Culture
    • Performance Center: Full AI gym suite, recovery modalities, group fitness classes, body composition tracking, and state-of-the-art aesthetic modalities.

    Job Type: Full-time
    Location: Albuquerque, New Mexico