Ampcus, Inc
Public Administration Analyst - Clinical Research
Ampcus, Inc, Los Angeles, California, United States, 90079
Description:Hybrid, but mostly remote.
700 Tiverton 8-684 Factor, Los Angeles, CA 90095
Candidate Questions:Must ask each candidate the following and include their answers on the BOTTOM of the cover sheet prior to submittal:Do you have experience creating and updating study protocol calendars and budgets in a CRMS or CTMS?If yes, which application?
Job Description:Under the direction of the Clinical Study Initiation Manager (CSI Manager) and Senior Leadership, the Clinical Study Initiation (CSI) Analyst is responsible for database management related to research trials and patient information. This includes building/updating research calendar specifications, calendars, and budgets, as well as ensuring the integrity of data collected and entered into the clinical research management system (CRMS). The position will monitor, verify, and validate the integrity of various data elements within the CRMS.
Qualifications:Required Experience:Experience working in the clinical research fieldExperience reviewing research protocols and developing clinical trial calendars and budgets in a Clinical Research Management System (CRMS) or Clinical Trial Management System (CTMS)Experience using MS Office Applications, particularly Excel and Word
Preferred Experience:Experience with Hematology/Oncology researchExperience using OnCore, Velos, or similar CRMSExperience creating a clinical research budget
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700 Tiverton 8-684 Factor, Los Angeles, CA 90095
Candidate Questions:Must ask each candidate the following and include their answers on the BOTTOM of the cover sheet prior to submittal:Do you have experience creating and updating study protocol calendars and budgets in a CRMS or CTMS?If yes, which application?
Job Description:Under the direction of the Clinical Study Initiation Manager (CSI Manager) and Senior Leadership, the Clinical Study Initiation (CSI) Analyst is responsible for database management related to research trials and patient information. This includes building/updating research calendar specifications, calendars, and budgets, as well as ensuring the integrity of data collected and entered into the clinical research management system (CRMS). The position will monitor, verify, and validate the integrity of various data elements within the CRMS.
Qualifications:Required Experience:Experience working in the clinical research fieldExperience reviewing research protocols and developing clinical trial calendars and budgets in a Clinical Research Management System (CRMS) or Clinical Trial Management System (CTMS)Experience using MS Office Applications, particularly Excel and Word
Preferred Experience:Experience with Hematology/Oncology researchExperience using OnCore, Velos, or similar CRMSExperience creating a clinical research budget
#J-18808-Ljbffr