Cancer Research Project Coordinator

UCLA
Los Angeles, CA Full Time
POSTED ON 10/10/2021 CLOSED ON 10/28/2021

What are the responsibilities and job description for the Cancer Research Project Coordinator position at UCLA?

We are seeking a highly motivated, dynamic and detail-oriented individual to join our team at the UCLA Center for Cancer Prevention and Control Research (CPCR) and the UCLA Kaiser Permanente Center for Health Equity (CHE) to serve as a Project Coordinator in our highly productive research group. Primary responsibilities will be related to a newly funded project focused on increasing colorectal cancer screening rates and the follow-up of abnormal screening results among Federally Qualified Health Center (FQHC) patients. The project is a national collaboration between researchers from UCLA, Dana Farber Cancer Center and Massachusetts General Hospital in Boston, and the Tribal Nations in South Dakota. The project is part of a very exciting funding opportunity and will include both formal research and public service towards reducing disparities in colorectal cancer nationally.

Under the general direction of the Principal Investigator and Co-Investigator, the Project Coordinator will manage the full range of research project activities including participation in planning and implementation of research activities at FQHC sites including data collection and intervention implementation; training and supervising part time project staff as needed; coordinating and managing data collection activities at FQHC sites; communicating regularly with staff at FQHCs and other academic study sites; maintaining detailed and accurate documentation of all research project activities; developing agendas, presentations and supporting documentation for research team meetings; maintaining all necessary UCLA IRB approvals; drafting progress and annual reports and plan updates required by the funding agency; actively participating in the development of presentations and manuscripts for academic and community audiences. Provide other research support as needed for project and other research efforts in the Centers.

Percentage of Time:
100

Shift Start:
8:00 am

Shift End:
5:00 pm

Qualifications for Position

20
Records

Qualifications

Required/Preferred

Advanced degree in public health or related field or an equivalent combination of education and experience.

Required

Demonstrated experience in program planning, implementation and evaluation.

Preferred

Research training and experience (required), including intervention research experience (preferred).

Required

Demonstrated experience with data collection and data entry.

Required

Working knowledge of cancer prevention and control research.

Preferred

Experience in working with safety net clinics, schools/pre-schools, or other community-based organizations.

Preferred

Strong organizational skills for of project planning, data collection procedures, and conduct of complex research activities. Ability to prioritize and effectively manage heavy workload with multiple, deadlines.

Required

Demonstrated oral communication skills to obtain and convey information accurately and precisely and to speak effectively and appropriately on a wide variety of job related subjects.

Required

Demonstrated written communication and proofreading skills to compose grammatically correct and content appropriate correspondence, proposals, reports, etc., and in editing written material for grammatical correctness.

Required

Demonstrated interpersonal skills to interact effectively and diplomatically with many different individuals at all organization levels, the lay and professional public, and to maintain effective and cooperative working relationships with staff and community members.

Required

Demonstrated analytical skills to recognize issues/situations that require action, define problems by performing research and fact finding, present alternatives in an analytical and logical format, and formulate, recommend, and implement solutions.

Required

Ability to work in diverse community settings with multicultural populations.

Required

Working knowledge of policies and procedures of Human Subjects related research.

Required

Working knowledge of Excel and experience working with output from Stata, SAS and/or similar quantitative software.

Preferred

Demonstrated ability to electronically maintain research and other data and experience with database and spreadsheet development.

Required

Ability to establish and maintain accurate electronic files and other records.

Required

Ability to travel between multiple project sites in the Los Angeles and San Fernando Valley areas.

Required

Ability to train and supervise staff.

Required

Bilingual (English/Spanish) skills.

Preferred

Ability to work occasional evenings and weekends as needed.

Required

Additional Posting Information

Bargaining Unit:
99-Policy Covered

Application Deadline:
10-22-2021

External Posting Date:
Clinical Research Coordinator
Matrix Clinical Research -
Los Angeles, CA
Senior Clinical Research Coordinator
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Inglewood, CA
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Lancaster, CA

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