Clinical Research Coordinator I - 134425

Davita Inc.; San Diego (CA); On-site; USD 66,000 - 108,000; Full time

Job summary

The Moores Cancer Center in San Diego is seeking a Clinical Research Coordinator I to manage clinical trials. This role involves protocol management, patient eligibility screening, data collection, and communication with clinical teams. Ideal candidates possess a Bachelor's degree and relevant clinical research experience in a dynamic environment.

Qualifications

• Experience in clinical research environments is essential.
• Proficiency with statistical software and data management is required.
• Fluency in English and another language is preferred.

Responsibilities

• Coordinate and manage clinical trials, including protocol management and data collection.
• Assist with regulatory submissions and monitor treatment and toxicities.
• Communicate with physicians and disease groups.

Skills

Knowledge of biology

Knowledge of clinical sciences

Organizational skills

Excellent communication skills

Ability to work independently

Education

Bachelor's degree or equivalent experience

Tools

Statistical software

MS Word

Excel

Velos

Access

Job description

The Moores Cancer Center (MCC) is one of just 57 NCI-designated Comprehensive Cancer Centers in the United States and the only one in San Diego County. As a consortium cancer center, it is a collaborative partnership between UCSD, encompassing 28 departments, 6 schools (School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, School of Public Health, Jacobs School of Engineering, School of Biological Sciences, & the School of Physical Sciences), UCSD Health oncology hospitals and clinics, San Diego State University (SDSU), and the La Jolla Institute of Immunology (LJI). These programs are dedicated to reducing cancer's burden and include research, patient care, outreach, and education. The MCC offers challenging career opportunities in a fast-paced, innovative environment, emphasizing career development, cross-training, and professional growth.

The Clinical Trials Office (CTO) at UCSD's MCC manages numerous clinical trials sponsored by NCI cooperative groups, pharmaceutical companies, and physician investigators.

Reporting to the Disease Team Project Manager, the Clinical Research Coordinator I will coordinate and manage clinical trials, including protocol management, patient eligibility screening, data collection, protocol compliance, adverse reaction reporting, monitoring treatment and toxicities, laboratory submissions, and maintaining research files. The role also involves assisting with regulatory submissions, communicating with physicians and disease groups, attending meetings, reviewing research accounts, and other duties as assigned.

Minimum Qualifications

• Knowledge of biology, microbiology, social sciences, and clinical sciences, typically gained through a Bachelor's degree or equivalent experience.
• Experience in clinical research environments.
• Proficiency with statistical software, databases, and office applications such as Velos, Access, Excel, and MS Word.
• Experience with laboratory procedures, patient eligibility assessment, and interpreting medical data.
• Familiarity with FDA policies regulating clinical trials.
• Experience in medical assessments and patient interviews related to protocol management.
• Ability to interpret medical charts and abstract data.
• Knowledge of NIH, GCP, IIPP, HRPP, IATA shipping, and Bloodborne Pathogens protocols.
• Experience recruiting clinical trial participants.
• Experience coordinating study startup activities.
• Ability to train research personnel on protocols and procedures.
• Understanding of diagnostic procedures like x-rays and scans.
• Strong organizational skills and ability to prioritize in a dynamic setting.
• Excellent communication skills, both written and verbal, including phone etiquette.
• Ability to work independently and maintain confidentiality.
• Experience completing clinical trial case report forms.
• Effective interaction with diverse groups, including staff and clients.

Preferred Qualifications

• Bachelor's degree or equivalent experience/training.
• Certification as a Clinical Research Associate or Coordinator.
• Fluency in English and at least one additional language such as Spanish, Korean, Vietnamese, Mandarin, or Cantonese.
• Experience with research bulk accounts and investigational drug authorization.

Special Conditions

• Subject to criminal background check and pre-employment physical.
• Willingness to travel, work weekends, and evenings as needed.
• Ability to obtain annual TB/Fit test clearances.

Pay Transparency Act

Annual Full Pay Range: $66,753 - $107,407 (prorated if less than full-time)

Hourly Range: $31.97 - $51.44

Compensation factors include experience, skills, knowledge, education, licensure, certifications, and organizational needs. The posted pay scale reflects the budgeted salary range, which may vary based on internal equity and other factors.