Clinical Research Data Coordinator I - 134002

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 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.

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 Data Coordinator I is responsible for coordinating and managing the ongoing collection, quality assurance, and analysis of data for low to moderately complex oncology clinical trials. Working in conjunction with the Clinical Research Coordinator (CRC), the Data Coordinator ensures timely and accurate data entry, reporting, and responsiveness to data queries. Assists with ongoing monitoring and quality assurance to ensure compliance with data requirements. Directly communicate with physicians and clinical staff to review study data and provide routine updates to the clinical research team. 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.

• Experience working with medical records to extract patient data and record data in approved format for study purposes (e.g., case report forms, data summaries).

• Experience interpreting medical charts and abstracting data from medical records.

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

• Demonstrated ability/experience to research and analyze data and then prepare concise, well-organized reports, summaries, and correspondence.

• Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately.

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

• 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.

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

• Ability to work independently. Ability to maintain confidentiality.

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

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

• Certification as a Clinical Research Associate or Coordinator.

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

• Experience with cancer-related research.

• Experience with Epic.

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

• Experience with clinical trial management systems.

• Access to transportation to off-site research locations.

• Possess and understands intercultural competence. Relevant to intercultural sensitivity to interact with people from diverse backgrounds.

• 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.

If employed by the University of California, you will be required to comply with our Policy on Vaccination Programs, which may be amended or revised from time to time. Federal, state, or local public health directives may impose additional requirements.

If applicable, life-support certifications (BLS, NRP, ACLS, etc.) must include hands-on practice and in-person skills assessment; online-only certification is not acceptable.

UC San Diego Health Sciences is comprised of our School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, The Herbert Wertheim School of Public Health and Human Longevity Science, and our Student Health and Well-Being Department. We have long been at the forefront of translational - or "bench-to-bedside" - research, transforming patient care through discovery and innovation leading to new drugs and technologies. Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care. We invite you to join our team!

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For the University of California's Affirmative Action Policy please visit: https://policy.ucop.edu/doc/4010393/PPSM-20
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Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.

a. "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer. For reference, below are UC's policies addressing some forms of misconduct:

• UC Sexual Violence and Sexual Harassment Policy
• UC Anti-Discrimination Policy
• Abusive Conduct in the Workplace