Clinical Research Coordinator II - 135689

Davita Inc.; San Diego (CA); On-site; USD 74,000 - 121,000; Full time

Job summary

A leading healthcare provider in San Diego is seeking a Clinical Research Coordinator II to manage and coordinate clinical trials. This pivotal role involves overseeing trial implementation, ensuring regulatory compliance, and educating the public and stakeholders about ongoing research efforts. Ideal candidates will have extensive experience in clinical trials and a background in relevant sciences.

Qualifications

• Six years of related experience, or a Bachelor's degree plus two years of related experience/training.
• Experience in clinical trials research, protocol design, data collection, and evaluation.
• Knowledge of investigational protocols, especially in oncology.

Responsibilities

• Oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of research subjects.
• Develop start-up procedures for phase I-III studies and ensure regulatory compliance.
• Educate the public about trials and assist PIs with reports and manuscripts.

Skills

Problem-solving

Communication

Organizational skills

Resourcefulness

Conflict resolution

Education

Bachelor's degree in a relevant field

Master's degree in social or basic sciences

Tools

Microsoft Office

Job description

UCSD Layoff from Career Appointment

Apply by 06/20/2025 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor.

Special Selection Applicants: Apply by 07/01/2025. Eligible Special Selection clients should contact their Disability Counselor for assistance.

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. It is a collaborative partnership involving UCSD, SDSU, LJI, and UCSD Health hospitals and clinics. The center is dedicated to reducing the burden of cancer through research, patient care, outreach, and education. It offers challenging career opportunities in a fast-paced, innovative environment, emphasizing career development, cross-training, and professional growth.

The Clinical Trials Office (CTO) at MCC manages numerous clinical trials sponsored by various entities, including NCI cooperative groups, pharmaceutical companies, and investigators.

The Clinical Research Coordinator (CRC) II will oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of research subjects. Responsibilities include creating informational materials, liaising with departments, developing start-up procedures for phase I-III studies, ensuring regulatory compliance, overseeing data quality, guiding investigators, educating the public about trials, assisting PIs with reports and manuscripts, creating documents and policies, and working with regulatory officials.

QUALIFICATIONS

• Six years of related experience, or a Bachelor's degree plus two years of related experience/training.
• Experience in clinical trials research, protocol design, data collection, and evaluation.
• Knowledge of study start-up, feasibility, IRB processes, budget negotiations, and invoicing.
• Experience in a clinical research environment such as CRO, academic institution, or research hospital.
• Ability to lead and assist in maintaining an efficient research team.
• Knowledge of investigational protocols, especially in oncology.
• Experience in patient eligibility screening, treatment initiation, specimen collection, and physician orientation.
• Proficiency in completing case report forms both hard copy and online.
• Resourcefulness and ability to establish contacts and find solutions.
• Ability to discern tasks requiring supervision and act promptly.
• Working knowledge of medical/scientific terminology.
• Problem-solving and conflict resolution skills.
• Excellent organizational and communication skills, tact, and diplomacy.
• Proficiency in Microsoft Office and internet research.
• Strong administrative and coordination skills.

PREFERRED QUALIFICATIONS

• Master's degree in social or basic sciences.
• Certification as a Clinical Research Coordinator.
• Fluency in English and at least one language among Spanish, Korean, Vietnamese, Mandarin, or Cantonese.
• Knowledge of cost accounting, medical billing, and collections.

SPECIAL CONDITIONS

• Background check and physical required.
• Ability to travel, work weekends/evenings, and obtain TB/Fit test clearances.

Pay Transparency Act

Annual Full Pay Range: $74,792 - $120,269 (prorated if less than 100% appointment)

Hourly Range: $35.82 - $57.60

Compensation depends on experience, skills, education, and organizational needs. The posted salary range reflects the budgeted range and may vary based on internal factors.