The Moores Cancer Center (MCC) is one of just 53 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 the 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; the basic and public health research and outreach of San Diego State University (SDSU), and the basic and translational research of the La Jolla Institute of Immunology (LJI). These various programs and units are all dedicated to fulfilling the Moores Cancer Center's mission of reducing cancer's burden. As such, it ranks among the top centers in the nation conducting the continuum of cancer research, providing advanced patient care, and serving the community through outreach and education programs. As a top-ranking, future-oriented organization, we offer challenging career opportunities in a fast-paced and innovative environment. Moores Cancer Center follows a progressive philosophy of career-path development for its employees including opportunities for cross-training, professional development, and progressive responsibility.

MCC's mission is to transform cancer care in our catchment area and beyond by driving exceptional scientific discoveries and innovations in prevention, detection, care, and training. MCC will make a global impact on improving health by reducing cancer burden through accelerated discovery and translation, compassionate andinterdisciplinary care, education and community engagement, with the foundation of our core values -Excellence, Innovation and Risk-Taking, Collaboration, Diversity and Service.

The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.

Reporting directly to the Disease Team Project Manager, the Long-Term Follow-Up Coordinator is responsible for coordinating and managing long-term follow-up patient care and data entry. Responsible for patient management, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient follow-up clinical care, laboratory and specimen submission, and maintenance of accurate and complete clinical research files. Assist the regulatory department with submissions, renewals, and safety reports. Directly communicate with assigned physicians and disease groups, including attending weekly meetings and tumor boards. Provide direct assistance to the Disease Team Project Manager in reviewing and verifying long-term follow-up patient care and data coordination. Other duties assigned as needed.

• Theoretical knowledge of biology, microbiology, social sciences, and clinical sciences as typically attained by a Bachelor's degree, or an equivalent combination of education and experience.

• Experience performing clinical research duties in a clinical research environment.

• Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource Protection Program (HRPP), IATA Shipping of Blood Specimens, and Bloodborne Pathogens.

• Working knowledge of computer software including Microsoft Office (Outlook, Word, Excel, and PowerPoint).

• Experience completing clinical trials case report forms via hard copy and online.

• Working knowledge of medical terminology. Knowledge of x-rays, scans, and other diagnosticprocedures.

• Access to transportation to off-site research locations.

• Demonstrated ability to research, properly evaluate information, and prepare concise, well organized reports, summaries, and correspondence.

• Excellent interpersonal, as well as written and verbal communication skills (using grammatically correct written English and accurate typing) to interact with a diverse population. Excellent phone etiquette skills.

• Demonstrated ability to interact effectively with diverse groups, including professional andnonprofessional staff and clients.

• Bachelor's degree in related area and / or equivalent experience / training.

• Certification as a Clinical Research Associate or Coordinator.

• Fluent in English and at least one of the following languages: Spanish, Tagalog, Korean, Vietnamese, Arabic, Mandarin or Cantonese.

• Experience with cancer-related research.

• Knowledge with various types of human subject clinical trials i.e., National Group, Industrial, and Investigator-authored.

• Experience with clinical trial management systems.

• Experience with electronic medical records, preferably Epic.

• Employment is subject to a criminal background check and pre-employment physical.

• Must be able to obtain annual TB/Fit test clearances.

• Must be able to travel to different locations and work weekends and eveningsas needed.