Lead Clinical Research Coordinator
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Job Description
Join the Southwest Women's Oncology Team:
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
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.