What are the responsibilities and job description for the Clinical Research Coordinator position at Serv Recruitment Agency?
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
