Clinical Research Coordinator-Per Diem

Eisenhower Health • Rancho Mirage, CA

95d • $37

About The Position

The position involves coordinating and implementing clinical research activities within the Research-Oncology department. The role requires a Bachelor’s degree in healthcare or a related field, along with specific training in Good Clinical Practice and Clinical Research Coordinator courses. The job entails working closely with patients, clinical trials, and various stakeholders to ensure compliance and quality in research activities.

Requirements

• Bachelor’s degree in healthcare and/or related field.
• Three (3) years current experience in acute care hospital, medical center, health system or related industry.
• Completion of CITI Program courses: Good Clinical Practice (GCP), Clinical Research Coordinator Foundations, Clinical Research Coordinator Advanced.

Nice To Haves

• Master’s degree.
• ACRP CCRC or SOCRA CCRP Certification.

Responsibilities

• Demonstrates compliance with Code of Conduct and compliance policies.
• Recruits, educates, consents, schedules, and completes follow-up with patients/subjects.
• Participates in the design, planning and conduct of clinical trials program and clinical research projects.
• Performs pre-investigation, initiation and periodic monitoring visits.
• Monitors subject records for quality, data integrity and compliance.
• Assists in writing and/or auditing clinical reports.
• Assists in developing protocols, case report forms, and informed consent documents.
• Acts as a liaison between sponsors, CRO sites and other department staff.
• Manages the negotiation and monitoring of budgets and contracts.
• Performs clinical site activities including regulatory issues and patient care coordination.
• Develops sufficient expertise to communicate directly with clinicians and staff.
• Contributes to the development of SOPs, best practices, and training.
• Manages tracking and reporting of Serious Adverse Events and Adverse Events.
• Works with physicians and leadership to develop and implement client trials.
• Facilitates research and enrollment to research studies and clinical trials.
• Prepares and presents materials to Institutional Review Board (IRB).
• Develops educational/promotional materials for patients.
• Coordinates performance improvement activities related to clinical trials.
• Provides support to investigators and maintains statistics on programs and trials.
• Develops and implements an Education Program for the community.
• Performs other duties as assigned.

What This Job Offers

• Education Level: Bachelor's degree
• Number of Employees: 1,001-5,000 employees