Assistant Clinical Research Coordinator - Cancer Immunotherapy Program
UCSF Health, San Francisco, CA, United States
Job Description
The Helen Diller Family Comprehensive Cancer Center (HDFCCC) Clinical Research Support Office (CRSO) is seeking a limited appointment Assistant Clinical Research Coordinator for the Cancer Immunotherapy Program to assist with the daily needs of our clinical trials. Under the supervision of a Clinical Research Supervisor, Clinical Research Manager, and/or Principal Investigator (PI), the incumbent will perform entry‑level duties related to the support and coordination of clinical studies and may receive training and development to prepare for advancement to journey‑level work within the series.
Qualifications
Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities, and/or equivalent experience/training.
Excellent verbal and written communication and presentation skills.
Excellent organizational and interpersonal skills to work effectively in a diverse team.
Attention to detail.
Proficiency with Microsoft Word, PowerPoint, and Windows.
Excellent analytical and problem‑solving skills.
Ability to work effectively in a fast‑paced, team‑based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
Ability to establish cooperative working relationships with patients, co‑workers, and physicians.
Preferred Qualifications
Demonstrated proficiency with medical terminology.
Experience working with patients or study subjects.
Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.
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The Helen Diller Family Comprehensive Cancer Center (HDFCCC) Clinical Research Support Office (CRSO) is seeking a limited appointment Assistant Clinical Research Coordinator for the Cancer Immunotherapy Program to assist with the daily needs of our clinical trials. Under the supervision of a Clinical Research Supervisor, Clinical Research Manager, and/or Principal Investigator (PI), the incumbent will perform entry‑level duties related to the support and coordination of clinical studies and may receive training and development to prepare for advancement to journey‑level work within the series.
Qualifications
Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities, and/or equivalent experience/training.
Excellent verbal and written communication and presentation skills.
Excellent organizational and interpersonal skills to work effectively in a diverse team.
Attention to detail.
Proficiency with Microsoft Word, PowerPoint, and Windows.
Excellent analytical and problem‑solving skills.
Ability to work effectively in a fast‑paced, team‑based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
Ability to establish cooperative working relationships with patients, co‑workers, and physicians.
Preferred Qualifications
Demonstrated proficiency with medical terminology.
Experience working with patients or study subjects.
Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.
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