University of California San Diego

Assistant Clinical Research Coord - Cancer Center - 141630

Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in biology, microbiology, social sciences, clinical sciences, or equivalent experience.
  • Clinical research experience in a research environment.
  • Knowledge of clinical research principles and protocols.
  • Ability to interpret medical charts and extract data from records.
  • Experience with various molecular biology techniques and sample handling.

Responsibilities

  • Assist in the initiation, implementation, and management of clinical studies.
  • Recruit and consent participants for clinical trials.
  • Collect and input research data accurately into systems.
  • Update and maintain study and patient records.
  • Submit protocol applications and amendments to the IRB.

Benefits

  • Opportunities for cross-training and professional development.
  • Access to a fast-paced, innovative work environment.
  • Career-path development focused on growth and responsibility.
  • Collaboration with a prestigious NCI-designated Comprehensive Cancer Center.
Full Job Description
Payroll Title:
CLIN RSCH CRD AST Department:
CANCER CENTER/Solid Tumor Therapeutics Hiring Pay Scale
$36.31 - $38.55 / Hour Worksite:
Moores Cancer Center Appointment Type:
Career Appointment Percent:
100% Union:
RX Contract Total Openings:
1 Work Schedule:
Days, 8-Hour Shifts, Monday-Friday

#141630 Assistant Clinical Research Coord - Cancer Center
Filing Deadline: Tue 10/13/2026
Apply Now

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 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 accelerateddiscovery and translation, compassionate and interdisciplinary care, education and community engagement, with the foundation of our core values - Excellence, Innovation and Risk-Taking, Collaboration, Diversity and Service.

Under general supervision, the Assistant Clinical Research Coordinator (ACRC) will work on clinical research projects for the Early Detection and Prevention Initiative, including studies focused on colorectal cancer, the Pancreatic Cancer Early Detection (PRECEDE) consortium study, and other studies relevant to early detection as needed. The ACRC will be responsible for various aspects of protocol management such as assisting with initiation, implementation, and management of clinical studies, recruiting and consenting participants, collecting and entering research data, updating study and patient records, submitting protocol applications and amendments to local IRB, sample acquisition and processing, and maintenance of accurate and complete research files. Other duties assigned as needed.

MINIMUM QUALIFICATIONS
  • Theoretical knowledge of biology, microbiology, social sciences, 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 clinical research protocols, principles, and standards.
  • Experience interpreting medical charts and abstracting data from medical records.
  • Ability to understand and interpret complex research protocols in order to screen patients for eligibility, initiate study plan, collect data, evaluate for adverse events and protocol deviations.
  • Ability to perform blood sample preparations including centrifugation, pipetting, making various buffer solutions, and proper sample storage. Ability to use biosafety cabinet, ULT/LN freezers, and centrifuge.
  • Skills in administering study related questionnaires and assessments.
  • Computer experience including Microsoft Office, database management and email skills.
  • Ability to accurately collect, record, transcribe and synthesize clinical data while paying conscientious attention to details.
  • Experience maintaining files and keeping records.
  • Ability to handle laboratory samples, learn and carry out shipping procedures.
  • Ability to communicate to supervisor, PI and research team study progress and accept constructive advice and suggestions.
  • Ability to work independently. Ability to maintain confidentiality.
  • Demonstrated ability to interact effectively with diverse groups, including professional and non-professional staff and clients.
  • 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.
  • 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.
  • Ability to understand and learn study procedures from protocols. Ability to problem-solve.
  • Ability to work with different clinical protocols concurrently.
  • Knowledge of Human Subjects Protection requirements.
  • Ability to perform molecular biology techniques including PCR, RT-PCR, cDNA synthesis, gene expression analysis, recombinant protein expression, RNA/DNA isolation, protein purification.
SPECIAL CONDITIONS
  • Employment is subject to a criminal background check and pre-employment physical.
  • Must be able to work various hours and locations based on business needs. Must be able to travel to different locations and work weekends and evenings as needed.
  • Must be able to obtain annual TB/Fit test clearances.
  • Ability and willingness to process blood samples.
Pay Transparency Act

Annual Full Pay Range: $75,815 - $121,960 (will be prorated if the appointment percentage is less than 100%)

Hourly Equivalent: $36.31 - $58.41

Factors in determining the appropriate compensation for a role include experience, skills, knowledge, abilities, education, licensure and certifications, and other business and organizational needs. The Hiring Pay Scale referenced in the job posting is the budgeted salary or hourly range that the University reasonably expects to pay for this position. The Annual Full Pay Range may be broader than what the University anticipates to pay for this position, based on internal equity, budget, and collective bargaining agreements (when applicable).

Apply Now

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.

About University of California San Diego

The University of California San Diego (UC San Diego) is a public research university in San Diego, California. Established in 1960 near the pre-existing Scripps Institution of Oceanography, UC San Diego is the seventh-oldest of the 10 University of California campuses and offers over 200 undergraduate and graduate degree programs, enrolling approximately 38,325 students. UC San Diego is organized into six undergraduate residential colleges (Revelle, John Muir, Thurgood Marshall, Earl Warren, Eleanor Roosevelt, and Sixth College) and five academic divisions (Arts and Humanities, Biological Sciences, Jacobs School of Engineering, Physical Sciences, and Social Sciences). The university operates 19 organized research units (ORUs), including the Center for Energy Research, Qualcomm Institute (a branch of the California Institute for Telecommunications and Information Technology), and the San Diego Supercomputer Center.
Learn more about University of California San Diego
Size
38,325 employees
Industry

Similar Jobs

More Jobs at University of California San Diego

More Healthcare Jobs

Find similar Assistant Clinical Research Coord - Cancer Center - 141630 jobs: